A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585919



Internal ID16373328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32933057..32981616hg38UCSC Ensembl
Innerchr20:31520863..31569422hg19UCSC Ensembl
Innerchr20:30984524..31033083hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3848560
hg1948560
hg1848560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939268
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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