A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585915



Internal ID16373324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32583046..32585037hg38UCSC Ensembl
Innerchr20:31170848..31172839hg19UCSC Ensembl
Innerchr20:30634509..30636500hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381992
hg191992
hg181992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7557n54
Supporting Variantsnssv939263, nssv939262, nssv939261
Samples
Known GenesC20orf112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585915
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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