A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585351



Internal ID16372760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6141205..6149930hg38UCSC Ensembl
Innerchr20:6121852..6130577hg19UCSC Ensembl
Innerchr20:6069852..6078577hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg388726
hg198726
hg188726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7452n54
Supporting Variantsnssv937570, nssv937571
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585351
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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