Variant Details

Variant: esv2664638

Internal ID

9584057

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chrX:155804633..155983132	hg38	UCSC Ensembl
Outer	chrX:155804476..155983285	hg38	UCSC Ensembl
Inner	chrX:155034296..155212797	hg19	UCSC Ensembl
Outer	chrX:155034139..155212950	hg19	UCSC Ensembl

Cytoband

Xq28

Allele length

Assembly	Allele length
hg38	178810
hg19	178812

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv1407e199

Supporting Variants

essv6220905, essv5822044, essv5718342, essv6227889, essv6254430, essv6247767, essv6230435, essv6274418, essv6194390, essv5504061, essv6265774, essv6423969, essv5752305, essv6167651, essv6229886, essv6408420, essv5830193, essv5998490, essv6396791, essv5822823, essv5925901, essv6327659, essv6167089, essv5991387, essv5695647, essv6544361, essv5798032, essv6235976, essv5496913, essv5951281, essv5961787, essv5731368, essv5746887, essv6475894, essv6183918, essv5721615, essv5590264, essv6350393, essv6269342, essv5717264, essv6379289, essv6042591, essv6509623, essv6051538, essv6550621, essv5536162, essv5467974, essv6229695, essv5623941, essv5529926, essv6207331, essv5662886, essv6117225, essv5552961, essv5452617, essv6001271, essv5950742, essv6062711, essv5640783, essv5877494, essv5728744, essv6590221, essv6445202, essv6573251, essv5505974, essv6052062, essv6153495, essv5582601, essv5714414, essv6518680, essv5686574, essv5899074, essv6520338, essv6057445, essv5513597, essv5833128, essv5775694, essv6556648, essv6015937, essv6014923

Samples

NA19648, NA18621, HG00249, NA19332, HG01066, HG00315, NA19350, NA19057, NA18596, NA19377, NA18606, NA19443, NA12400, NA19067, HG01140, HG00271, NA19107, NA19068, NA18595, NA18619, NA12348, NA19313, HG00139, HG01067, NA18874, HG00232, HG00422, NA18557, NA19445, NA18908, NA18867, HG00419, NA18638, HG00154, NA18544, NA19247, HG00443, NA19462, NA18637, NA18579, NA19064, NA18548, HG00740, NA18566, HG00651, NA19084, NA06989, NA18853, NA19059, HG00152, NA18536, HG00246, NA18576, NA20799, NA18632, HG00155, NA18535, NA18543, NA19434, NA18950, NA19010, NA19835, HG01137, HG00319, NA18610, HG00339, NA19248, NA19472, HG01055, NA18636, NA18873, NA11843, NA18983, NA19004, NA19312, NA18549, NA18487, HG00437, NA20509, NA18620

Known Genes

VAMP7

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2664638

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	80
Observed Complex	0
Frequency	n/a