A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692990



Internal ID15082956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77011969..77076340hg38UCSC Ensembl
Innerchr15:77304310..77368682hg19UCSC Ensembl
Innerchr15:75091365..75155737hg18UCSC Ensembl
Innerchr15:75091365..75155737hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3864372
hg1964373
hg1864373
hg1764373
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517068
Supporting Variants
Samples
Known GenesPSTPIP1, TSPAN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692990
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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