A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586285



Internal ID16373694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55090083..55162620hg38UCSC Ensembl
Innerchr20:53706622..53779159hg19UCSC Ensembl
Innerchr20:53140029..53212566hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3872538
hg1972538
hg1872538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151374
Samples1780862373_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586285
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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