Variant Details

Variant: esv2664457

Internal ID

9930562

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chrX:81805917..81811823	hg38	UCSC Ensembl
Outer	chrX:81805396..81812493	hg38	UCSC Ensembl
Inner	chrX:81061416..81067322	hg19	UCSC Ensembl
Outer	chrX:81060895..81067992	hg19	UCSC Ensembl

Cytoband

Xq21.1

Allele length

Assembly	Allele length
hg38	7098
hg19	7098

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5601570, essv6571340, essv5849547, essv5919255, essv5779894, essv5665459, essv6428262, essv5950349, essv6472151, essv6026016, essv5452061, essv6208841, essv5805680, essv5886936, essv5537187, essv6033272, essv5467653, essv6359098, essv6229767, essv5870530, essv6179414, essv5995746, essv5398777, essv6535852, essv5682694, essv6025178, essv6470441, essv5917087, essv5866810, essv5481266, essv6066185, essv6449013, essv6595646, essv5631463, essv6396094, essv5737929, essv6102077, essv6565931, essv6255024, essv6509319, essv6145676, essv5628456, essv6212129, essv6118846, essv5999056, essv6490087, essv6086417, essv5844066, essv5669163, essv6014397, essv6517082, essv5403152, essv6408279, essv6106210, essv6073921, essv5706156, essv6215670, essv6097814, essv5569009, essv5491961, essv6401917, essv6182302, essv5879137, essv5409294, essv5847473, essv6505355, essv6370437, essv5864836, essv5651939, essv5695717, essv5790382, essv5529687, essv5515287, essv6580924, essv6422730, essv5756939, essv5462259, essv5699688, essv6311643, essv6064901, essv6260896, essv6030560, essv5728092, essv5978552, essv6437958, essv5576786, essv5485127, essv5592036, essv5893994, essv5600587, essv5929557, essv6224103, essv6263587, essv5990587, essv6178590, essv5649638, essv6427036, essv6413971, essv5893597, essv6388190, essv5848644, essv5948990, essv6384146, essv5940210, essv5498221, essv6307155, essv5890415, essv5539086, essv5780999, essv5554756, essv5830622, essv5585493, essv5400019, essv6277101, essv5395983, essv5609701, essv5771434, essv6596068, essv6162733, essv6365105, essv5661764, essv5416600, essv6373592, essv5834629, essv5449998, essv6451072, essv6116942, essv5959866, essv6334229, essv6262089, essv6499791, essv5761929, essv6487329, essv5566756, essv6280505, essv5691003, essv6420385, essv5772880, essv6446936, essv6170640, essv5428490, essv5463851, essv6035026, essv6058730, essv5987999, essv6002104

Samples

HG00593, HG00626, HG00403, HG00189, HG00650, HG00542, HG00442, HG00592, HG01356, HG00536, HG00608, HG00671, HG00361, HG01359, HG00559, HG00524, HG00187, HG01389, HG01374, HG00306, HG00367, HG01456, HG00566, HG00179, HG00177, HG01461, HG01140, HG00271, HG01250, HG01350, HG01366, HG00589, HG00272, HG01488, HG00702, HG00689, HG00448, HG00173, HG00634, HG00610, HG00369, HG00270, HG01365, HG00185, HG00311, HG00590, HG00512, HG00277, HG01455, HG00683, HG00335, HG00325, HG01440, HG00182, HG00427, HG00338, HG00178, HG01550, HG00530, HG01124, HG01353, HG01136, HG00188, HG00560, HG00629, HG01360, HG00266, HG00183, HG00176, HG00596, HG00328, HG00190, HG00653, HG00577, HG00701, HG00475, HG00436, HG00556, HG00533, HG00583, HG00500, HG01149, HG00619, HG00692, HG00635, HG00284, HG00273, HG00651, HG00373, HG01383, HG00613, HG00321, HG01497, HG00704, HG00463, HG01148, HG00611, HG00336, HG00625, HG00565, HG00366, HG00353, HG00580, HG00375, HG00357, HG01551, HG01253, HG00278, HG01494, HG00607, HG01113, HG01137, HG00662, HG00418, HG00620, HG00269, HG00707, HG00672, HG00614, HG00478, HG01491, HG00312, HG00421, HG00329, HG00656, HG00342, HG00267, HG01254, HG00174, HG00310, HG00186, HG00698, HG00280, HG00377, HG00372, HG00274, HG01377, HG00595, HG00472, HG01125, HG00628, HG00171, HG00345, HG01112, HG00180, HG01437

Known Genes

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)

esv2664457

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	146
Observed Complex	0
Frequency	n/a