A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589459



Internal ID16376868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5315847..5521684hg38UCSC Ensembl
Innerchr3:5357532..5563371hg19UCSC Ensembl
Innerchr3:5332532..5538371hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38205838
hg19205840
hg18205840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8186n54
Supporting Variantsnssv958054
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589459
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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