A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685725



Internal ID15422377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:47083787..47093148hg38UCSC Ensembl
Innerchr13:47657922..47667283hg19UCSC Ensembl
Innerchr13:46555923..46565284hg18UCSC Ensembl
Innerchr13:46555923..46565284hg17UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg389362
hg199362
hg189362
hg179362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519317
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685725
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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