A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585291



Internal ID16372700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3835007..3845429hg38UCSC Ensembl
Innerchr20:3815654..3826076hg19UCSC Ensembl
Innerchr20:3763654..3774076hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3810423
hg1910423
hg1810423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7443n54
Supporting Variantsnssv937359
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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