A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590613



Internal ID16378022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71890734..71951868hg38UCSC Ensembl
Innerchr3:71939885..72001019hg19UCSC Ensembl
Innerchr3:72022575..72083709hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3861135
hg1961135
hg1861135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965557
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590613
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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