Variant Details

Variant: esv2663210

Internal ID

9929315

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chrX:1603683..1604072	hg38	UCSC Ensembl
	chrX:1722576..1722965	hg19	UCSC Ensembl

Cytoband

Xp22.33

Allele length

Assembly	Allele length
hg38	390
hg19	390

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv1391e199

Supporting Variants

essv5498895, essv6145588, essv5588807, essv6310894, essv6009068, essv5960836, essv6298391, essv6504409, essv6139210, essv6536081, essv6206182, essv5992564, essv5881449, essv5562121, essv5404219, essv6191875, essv6206000, essv6008285, essv6030086, essv5408931, essv6566751, essv5407069, essv6051982, essv5955810, essv6349886, essv6344976, essv5957784, essv6390753, essv6417725, essv5783492, essv6331018, essv6446760, essv5983955, essv6257488, essv5978608, essv6056816, essv5728572, essv6432269, essv5835561, essv6598085, essv5412340, essv6038475, essv6474613, essv6491431, essv5884989, essv6471349, essv6028363, essv6412346, essv5836460, essv6429682, essv5761782, essv6402199, essv5991996, essv6281189, essv5584398, essv6104046, essv5493717, essv6039172, essv6461817, essv5923508, essv6527158, essv6501367, essv6281957, essv5631930, essv5800987, essv5996721, essv6090243, essv6477260, essv5514195, essv5479446, essv6516450

Samples

HG00114, NA18621, HG00142, HG01359, NA19359, NA19355, NA19057, NA20507, NA18526, NA18510, NA07346, NA19381, NA19728, HG00448, NA20795, NA18619, NA18960, NA18942, NA11918, NA20540, NA19313, NA19384, NA19079, HG00590, NA20539, NA19383, HG00335, NA11932, HG00705, NA18985, NA20757, HG00464, HG01124, NA11831, NA18613, NA19082, HG01384, NA19077, HG00584, HG00344, HG00692, NA18548, HG00284, HG00331, NA18532, NA12827, HG01334, NA19009, NA19469, NA18634, NA20765, NA18546, HG00258, HG00611, NA18632, NA19834, NA18517, NA19380, HG01375, HG01494, HG00256, HG00707, NA19716, HG01055, HG00343, NA18989, HG01082, NA19463, HG01112, NA18562, HG00581

Known Genes

ASMT

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2663210

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	71
Observed Complex	0
Frequency	n/a