A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586287



Internal ID16373696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55431443..55478773hg38UCSC Ensembl
Innerchr20:54047981..54095311hg19UCSC Ensembl
Innerchr20:53481388..53528718hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3847331
hg1947331
hg1847331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941577
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586287
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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