A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151747



Internal ID15877700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20438761..20563810hg38UCSC Ensembl
Innerchr3:20480253..20605302hg19UCSC Ensembl
Innerchr3:20455257..20580306hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38125050
hg19125050
hg18125050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589865
Supporting Variants
SamplesHGDP01031
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151747
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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