A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591961



Internal ID16379370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146676307..147007430hg38UCSC Ensembl
Innerchr3:146394094..146725217hg19UCSC Ensembl
Innerchr3:147876784..148207907hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38331124
hg19331124
hg18331124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976374
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591961
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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