A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572376



Internal ID16359785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34987083..35301212hg38UCSC Ensembl
Innerchr16:34221454..34535583hg19UCSC Ensembl
Innerchr16:34078955..34393084hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38314130
hg19314130
hg18314130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150555
SamplesHGDP00535
Known GenesUBE2MP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572376
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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