A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586309



Internal ID16373718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56833797..56856515hg38UCSC Ensembl
Innerchr20:55408853..55431571hg19UCSC Ensembl
Innerchr20:54842260..54864978hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3822719
hg1922719
hg1822719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7617n54
Supporting Variantsnssv941608, nssv941607
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586309
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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