Variant Details

Variant: esv2666278

Internal ID

9585697

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chrX:153641962..153644268	hg38	UCSC Ensembl
Outer	chrX:153641591..153644638	hg38	UCSC Ensembl
Inner	chrX:152907416..152909722	hg19	UCSC Ensembl
Outer	chrX:152907045..152910092	hg19	UCSC Ensembl

Cytoband

Xq28

Allele length

Assembly	Allele length
hg38	3048
hg19	3048

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6557834, essv6011769, essv6218901, essv6512253, essv5970207, essv6596086, essv6350245, essv6289998, essv5694354, essv6039375, essv5723830, essv5939878, essv6079677, essv5960867, essv5821080, essv5625797, essv5530433, essv6323080, essv5568657, essv5726074, essv6335676, essv5658729, essv6202463, essv6360951, essv5435263, essv5859349, essv6589046, essv6022944, essv5763325, essv5962169, essv5875642, essv5828613, essv5828020, essv5957225, essv6040653, essv6153526, essv5812585, essv6522887, essv5837794, essv6113213, essv5812111, essv5482576, essv6016143, essv6287056, essv6182277, essv5900269, essv6209851

Samples

NA19648, NA19664, NA19777, NA19684, NA19660, NA19762, NA19728, NA19678, NA19723, NA19771, NA19782, NA19681, NA19720, NA19719, NA19722, NA19725, NA19789, NA19717, NA19663, NA19788, NA19776, NA19654, NA19774, NA19655, NA19750, NA19761, NA19682, NA19756, NA19675, NA19685, NA19729, NA19652, NA19747, NA19732, NA19773, NA19679, NA19786, NA19783, NA19759, NA19785, NA19779, NA19716, NA19726, NA19780, NA19661, NA19758, NA19676

Known Genes

DUSP9

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2666278

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	47
Observed Complex	0
Frequency	n/a