A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589863



Internal ID16377272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20399695..20459911hg38UCSC Ensembl
Innerchr3:20441187..20501403hg19UCSC Ensembl
Innerchr3:20416191..20476407hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3860217
hg1960217
hg1860217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8251n54
Supporting Variantsnssv959884
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589863
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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