A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585982



Internal ID16373391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40011715..40030563hg38UCSC Ensembl
Innerchr20:38640357..38659205hg19UCSC Ensembl
Innerchr20:38073771..38092619hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3818849
hg1918849
hg1818849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939403
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585982
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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