A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585326



Internal ID16372735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5316005..5318022hg38UCSC Ensembl
Innerchr20:5296651..5298668hg19UCSC Ensembl
Innerchr20:5244651..5246668hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg382018
hg192018
hg182018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937455
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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