A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571686



Internal ID16359095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23148799..23152133hg38UCSC Ensembl
Innerchr16:23160120..23163454hg19UCSC Ensembl
Innerchr16:23067621..23070955hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383335
hg193335
hg183335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4957n54
Supporting Variantsnssv854162
Samples
Known GenesUSP31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571686
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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