A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571403



Internal ID16012126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8445407..8552076hg38UCSC Ensembl
Innerchr16:8495409..8602078hg19UCSC Ensembl
Innerchr16:8435410..8542079hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38106670
hg19106670
hg18106670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4901n54
Supporting Variantsnssv1150515, nssv1150514
SamplesHGDP00407, HGDP00438
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571403
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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