Variant Details

Variant: esv2673467

Internal ID

9939572

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr6:32550539..32573745	hg38	UCSC Ensembl
Outer	chr6:32550168..32574115	hg38	UCSC Ensembl
Inner	chr6:32518316..32541522	hg19	UCSC Ensembl
Outer	chr6:32517945..32541892	hg19	UCSC Ensembl

Cytoband

6p21.32

Allele length

Assembly	Allele length
hg38	23948
hg19	23948

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv1107e199

Supporting Variants

essv5753920, essv6494838, essv5805223, essv6571067, essv5950584, essv6380571, essv5842253, essv6441378, essv6270496, essv6411041, essv5496028, essv5440506, essv5501879, essv6550007, essv6151926, essv5755430, essv5971864, essv6418264, essv6180006, essv6541293, essv6493386, essv6240609, essv5914927, essv6073801, essv6304630, essv6545835, essv6212944, essv6214833, essv6389826, essv6148339, essv5831800, essv6538066, essv6427882, essv5923745, essv6083649, essv6065502, essv5627788, essv6458340, essv6329546, essv6235079, essv5902320, essv5871212, essv5446026, essv6148828, essv5856985, essv6201229, essv6177912, essv5688784, essv5940818, essv5948291

Samples

HG00189, HG00315, HG00306, HG00367, HG00318, HG00181, HG00177, HG00337, HG00327, HG00271, HG00272, HG00173, HG00330, HG00369, HG00270, HG00334, HG00281, HG00277, HG00335, HG00325, HG00326, HG00178, HG00188, HG00183, HG00176, HG00328, HG00190, HG00368, HG00320, HG00284, HG00373, HG00331, HG00321, HG00285, HG00366, HG00357, HG00278, HG00339, HG00312, HG00342, HG00267, HG00174, HG00186, HG00280, HG00343, HG00372, HG00274, HG00171, HG00345, HG00180

Known Genes

HLA-DRB6

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2673467

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	50
Observed Complex	0
Frequency	n/a