A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704017



Internal ID15093983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25679392..25680048hg38UCSC Ensembl
Innerchr15:25924539..25925195hg19UCSC Ensembl
Innerchr15:23475632..23476288hg18UCSC Ensembl
Innerchr15:23475632..23476288hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38657
hg19657
hg18657
hg17657
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527556
Supporting Variants
Samples
Known GenesATP10A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704017
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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