A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693032



Internal ID15082998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34450532..34462473hg38UCSC Ensembl
Innerchr15:34742733..34754674hg19UCSC Ensembl
Innerchr15:32530025..32541966hg18UCSC Ensembl
Innerchr15:32530025..32541966hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811942
hg1911942
hg1811942
hg1711942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693032
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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