A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571267



Internal ID16358676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3880210..3881088hg38UCSC Ensembl
Innerchr16:3930211..3931089hg19UCSC Ensembl
Innerchr16:3870212..3871090hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38879
hg19879
hg18879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4879n54
Supporting Variantsnssv852286, nssv852285, nssv852284
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571267
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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