A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150555



Internal ID15874405
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 StatusS
Merged Variantsnsv572376
Supporting Variants
SamplesHGDP00535
Known GenesUBE2MP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150555
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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