A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519663



Internal ID15446956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48446024..48455476hg38UCSC Ensembl
Innerchr16:48479935..48489387hg19UCSC Ensembl
Innerchr16:47037436..47046888hg18UCSC Ensembl
Innerchr16:47037436..47046888hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg389453
hg199453
hg189453
hg179453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696979
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519663
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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