A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585288



Internal ID16372697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3835007..3843697hg38UCSC Ensembl
Innerchr20:3815654..3824344hg19UCSC Ensembl
Innerchr20:3763654..3772344hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg388691
hg198691
hg188691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7443n54
Supporting Variantsnssv937353
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585288
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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