Is it probably safe to say I'm HV0f?

crazydude

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23 and me and wegene say I'm R0, but knowing how rare it is in Europeans makes me skeptical of those results.

Put my data into jameslick and these are the results the come.

Markers found (shown as differences to rCRS):

HVR2: 65D 191D 263G 299I 459D
CR: 613G 1438G 1646G 2074I 2156D 2405D 2706G 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7028T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 8860G 9716C 10256C 12184G 12208G 15198T 15514C
HVR1:

IMPORTANT NOTE: The above marker list is almost certainly incomplete due to limitations of genotyping technology and is not comparable to mtDNA sequencing results. It should not be used with services or tools that expect sequencing results, such as mitosearch.

Best mtDNA Haplogroup Matches:
1) HV0f

Defining Markers for haplogroup HV0f:
HVR2: 195C 263G
CR: 750G 1438G 2706G 4769G 7028T 8706G 8860G 15326G
HVR1: 16298C


Marker path from rCRS to haplogroup HV0f (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 72C 16298C ⇨ HV0 ⇨ 195C ⇨ HV0(T195C) ⇨ 72T 8706G ⇨ HV0f ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C

Imperfect Match. Your results contained differences with this haplogroup:
Matches(6): 72T 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(6): 195 750 4769 8706 15326 16298

2) HV
Defining Markers for haplogroup HV:
HVR2: 263G
CR: 750G 1438G 2706G 4769G 7028T 8860G 15326G
HVR1:


Marker path from rCRS to haplogroup HV (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C

Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(3): 750 4769 15326

2) HV(T16311C)
Defining Markers for haplogroup HV(T16311C):
HVR2: 263G
CR: 750G 1438G 2706G 4769G 7028T 8860G 15326G
HVR1: 16311C


Marker path from rCRS to haplogroup HV(T16311C) (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 16311C ⇨ HV(T16311C) ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C


Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(4): 750 4769 15326 16311

2) R0
Defining Markers for haplogroup R0:
HVR2: 263G
CR: 750G 1438G 2706G 4769G 7028T 8860G 14766T 15326G
HVR1:

Marker path from rCRS to haplogroup R0 (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 14766T ⇨ R0 ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C

Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(4): 750 4769 14766 15326

2) HV13
Defining Markers for haplogroup HV13:
HVR2: 263G
CR: 750G 1438G 2706G 4769G 7028T 8860G 15326G
HVR1: 16357C


Marker path from rCRS to haplogroup HV13 (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 16357C ⇨ HV13 ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C


Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(4): 750 4769 15326 16357

3) HV4
Defining Markers for haplogroup HV4:
HVR2: 263G
CR: 750G 1438G 2706G 4769G 7028T 7094C 8860G 15326G
HVR1:

Marker path from rCRS to haplogroup HV4 (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 7094C ⇨ HV4 ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C

Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
No-Calls(1): 7094C
Untested(3): 750 4769 15326

3) HV10
Defining Markers for haplogroup HV10:
HVR2: 263G
CR: 750G 1438G 2706G 4769G 7028T 8860G 13449T 15326G
HVR1: 16311C

Marker path from rCRS to haplogroup HV10 (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 16311C ⇨ HV(T16311C) ⇨ 13449T ⇨ HV10 ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C


Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(5): 750 4769 13449 15326 16311

3) HV18
Defining Markers for haplogroup HV18:
HVR2: 263G
CR: 750G 1438G 2706G 4769G 7028T 8860G 9039A 15326G
HVR1: 16189C

Marker path from rCRS to haplogroup HV18 (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 9039A 16189C ⇨ HV18 ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C

Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(5): 750 4769 9039 15326 16189

3) HV24
Defining Markers for haplogroup HV24:
HVR2: 263G
CR: 750G 1438G 1601T 2706G 4769G 7028T 8860G 15326G
HVR1: 16311C

Marker path from rCRS to haplogroup HV24 (plus extra markers):
H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 16311C ⇨ HV(T16311C) ⇨ 1601T ⇨ HV24 ⇨ 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C


Imperfect Match. Your results contained differences with this haplogroup:
Matches(5): 263G 1438G 2706G 7028T 8860G
Extras(32): 65D 191D 299I 459D 613G 1646G 2074I 2156D 2405D 3377G 3734G 3947G 4296A 4317I 4410T 5533G 5537D 5752D 5815T 7471D 7527A 7672T 8281D 8286D 8364G 8703T 9716C 10256C 12184G 12208G 15198T 15514C
Untested(5): 750 1601 4769 15326 16311
 

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