A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586651



Internal ID16374060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63830660..63836068hg38UCSC Ensembl
Innerchr20:62462013..62467421hg19UCSC Ensembl
Innerchr20:61932457..61937865hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385409
hg195409
hg185409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7686n54
Supporting Variantsnssv943893
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586651
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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