A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662948



Internal ID15052914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68513090..68529908hg38UCSC Ensembl
Innerchr15:68805429..68822247hg19UCSC Ensembl
Innerchr15:66592483..66609301hg18UCSC Ensembl
Innerchr15:66592483..66609301hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3816819
hg1916819
hg1816819
hg1716819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516489
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662948
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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