A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520443



Internal ID15447736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86088918..86089622hg38UCSC Ensembl
Innerchr16:86122524..86123228hg19UCSC Ensembl
Innerchr16:84680025..84680729hg18UCSC Ensembl
Innerchr16:84680025..84680729hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38705
hg19705
hg18705
hg17705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697423
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520443
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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