A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520679



Internal ID15447972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58976211..59084332hg38UCSC Ensembl
Innerchr15:59268410..59376531hg19UCSC Ensembl
Innerchr15:57055702..57163823hg18UCSC Ensembl
Innerchr15:57055702..57163823hg17UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38108122
hg19108122
hg18108122
hg17108122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv151n21
Supporting Variantsnssv697553
Samples
Known GenesRNF111
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520679
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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