A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673394



Internal ID15063360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61910283..62047927hg38UCSC Ensembl
Innerchr15:62202482..62340126hg19UCSC Ensembl
Innerchr15:59989774..60127418hg18UCSC Ensembl
Innerchr15:59989774..60127418hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38137645
hg19137645
hg18137645
hg17137645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516639
Supporting Variants
Samples
Known GenesVPS13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673394
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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