A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586694



Internal ID16374103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63835962..63842351hg38UCSC Ensembl
Innerchr20:62467315..62473704hg19UCSC Ensembl
Innerchr20:61937759..61944148hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg386390
hg196390
hg186390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944020
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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