A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589460



Internal ID16376869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5315847..5600268hg38UCSC Ensembl
Innerchr3:5357532..5641955hg19UCSC Ensembl
Innerchr3:5332532..5616955hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38284422
hg19284424
hg18284424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958055, nssv958056
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589460
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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