A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589932



Internal ID16030655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21943925..22006442hg38UCSC Ensembl
Innerchr3:21985417..22047934hg19UCSC Ensembl
Innerchr3:21960421..22022938hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3862518
hg1962518
hg1862518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960096
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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