A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662319



Internal ID9928424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2776388..2890783hg38UCSC Ensembl
chrX:2694429..2808824hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38114396
hg19114396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1392e199
Supporting Variantsessv6104853, essv5476286, essv5599733, essv5756703, essv6410123, essv6286273, essv5995310, essv6431133, essv6080960, essv6334277, essv5957902, essv6444396, essv5843387, essv6261126, essv5657629, essv6563259, essv6107426, essv6311696, essv5739825, essv5557077, essv5893890, essv5716216, essv6014816
SamplesHG01188, HG01140, HG00689, NA20586, NA19651, NA18868, HG00262, NA19372, HG01133, HG01124, NA18614, HG01136, NA19908, NA18538, NA19982, HG00331, NA19436, HG00638, HG00662, HG00707, HG00343, NA19063, NA18487
Known GenesGYG2, XG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662319
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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