A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589771



Internal ID16377180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14282349..14358256hg38UCSC Ensembl
Innerchr3:14323849..14399756hg19UCSC Ensembl
Innerchr3:14298853..14374760hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3875908
hg1975908
hg1875908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959440
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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