A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586865



Internal ID16374274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64315743..64333832hg38UCSC Ensembl
Innerchr20:62947096..62965185hg19UCSC Ensembl
Innerchr20:62417540..62435629hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3818090
hg1918090
hg1818090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7725n54
Supporting Variantsnssv944743, nssv944742, nssv944744
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586865
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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