A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586036



Internal ID16373445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:43848444..43854758hg38UCSC Ensembl
Innerchr20:42477084..42483398hg19UCSC Ensembl
Innerchr20:41910498..41916812hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386315
hg196315
hg186315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940522
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586036
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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