A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697779



Internal ID15434431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128394920..128532424hg38UCSC Ensembl
InnerchrX:127528898..127666402hg19UCSC Ensembl
InnerchrX:127356579..127494083hg18UCSC Ensembl
InnerchrX:127254433..127391937hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38137505
hg19137505
hg18137505
hg17137505
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521085
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697779
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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