A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699374



Internal ID15089340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61962790..61967438hg38UCSC Ensembl
Innerchr15:62254989..62259637hg19UCSC Ensembl
Innerchr15:60042281..60046929hg18UCSC Ensembl
Innerchr15:60042281..60046929hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384649
hg194649
hg184649
hg174649
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)nssv699374
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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