A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518393



Internal ID15445686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33272281..33284682hg38UCSC Ensembl
Innerchr15:33564482..33576883hg19UCSC Ensembl
Innerchr15:31351774..31364175hg18UCSC Ensembl
Innerchr15:31351774..31364175hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3812402
hg1912402
hg1812402
hg1712402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695823
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518393
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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