A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586286



Internal ID16373695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55189455..55402163hg38UCSC Ensembl
Innerchr20:53805994..54018701hg19UCSC Ensembl
Innerchr20:53239401..53452108hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38212709
hg19212708
hg18212708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941576
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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