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Lineages and Results of Y-chromosome DNA Testing for Surname CORBIN
and Variations, such as, CORBEN, CORBAN, CORBON, CORBYN, CORBINE, etc.
Haplogroup G
Results
Hub		 Y-DNA Haplogroups Represented in the Project
(n = number tested / number of progenitors)		 Project
Home
 G  (n = 2 / 1) I1 (n = 8 / 2) R1b (n = 17 / 7)
Haplogroup G is relatively uncommon (about 2.5% of tested Europeans).  G2a is not well understood, but is believed to have originated in Central Asia, then to have spread to the Middle East.  From there, it became widespread in Europe during the Neolithic.  The G2a subclade is found occasionally among Scandinavians.

We have two matching members who are Haplogroup G.  One of them has been deep SNP tested with the result that he is Haplogroup G2a.
Haplogroup G Subclades as Defined by SNP Mutations
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Red labels indicate markers that typically mutate more frequently than those labeled in black.
(Empty cells that are darkened indicate tests not ordered.)
Haplogroup G2a = G-P15
To view lineages, please scroll to the right.
Surname Kit # Ysearch
UserID		 Most
Downstream
Positive
SNP
Actually
Tested		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0		 19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
Modal values for Haplogroup G 14 22 15 10 14 14 11 12 11 12 11 29 16 9  9 11 11 23 16 21 31 12 13 13 14 10 11 20 20 15 13 15 18 36 38 11 10                                                             As per Whit Athey (as of 17 Dec 2006); characteristic markers highlighted in orange.
Modals for central European subclade G2a 14 22 15 10 13 14 11 13 11 12 11 29 17 9  9 11 11 24 16 21 31 12 13 13 14 10 11 20 20 15 13 15 18 36 38 11 10                                                             As per C.J. Swärdenheim, Admin., Scandinavian Project (as of 17 Dec 2006); differences from G highlighted in blue.
                 
CORBIN 36840 -   14 22 15 10 13 14 11 13 12 12 11 29 16 9 10 11 11 23 16 21 32 12 13 13 14                                                                                     Pvt10, Eugene Milo9, Daniel Edwin8, Milo H.7, Daniel6, Daniel5, Elijah4, Clement3, James2, Clement1 CORBIN — of Woodstock, CT
CORBAN 76227 FHEQK P15 14 22 15 10 13 14 11 13 12 12 11 29 16 9 10 11 11 23 16 21 32 12 13 13 14 10 10 20 20 15 13 17 17 35 38 11 10 11 8 15 16 8 11 10 8 11 11 14 22 22 14 10 12 12 15 8 13 21 22 19 12 11 13 11 11 11 12 Pvt7, Ralph Edmund6, George Wellington5, Josiah Barnum CORBAN4, Nathan Gregory3, Philip2, Philip1 CORBIN — of Danbury, CT
Our subjects have a few matches at 12 markers (in other surnames), but at 25-markers or higher, their haplotype is unique, matching only each other.  These test results support that Philip CORBIN of Danbury, CT, is closely related to (and most likely descended from) Clement CORBIN of Woodstock, CT.  Your project admin would like to encourage #36850 to upgrade his testing to 67 markers, so we can see just how closely these two are related.
Member #76227 has been deep SNP tested, with these results:
M201+ P15+ M285- M342- P20- M286- M287- M377- 
M201+ proves he is Haplogroup G; P15+ proves he is Haplgroup G2a.  The negative results for the other SNPs redundantly support that he was not any other subclade of G at the time he was tested.
   
What constitutes a match?
Matches in other surnames are usually mere coincidence, so please ignore them — I'll let you know when you shouldn't!
For 12 markers:  9 or less is a non-relative; 10-12, please see this Chart compiled by FTDNA.
For 25 markers:  21 or less is a non-relative; 22-25, please see this Chart compiled by FTDNA.
For 37 markers:  31 or less is a non-relative; 32-37, please see this Chart compiled by FTDNA.
For 67 markers:  55 or less is a non-relative; 56-67, please see this Chart compiled by FTDNA.
For any test:  0 matching markers, please contact NASA.

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