A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585918



Internal ID16026641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32851403..32956284hg38UCSC Ensembl
Innerchr20:31439209..31544090hg19UCSC Ensembl
Innerchr20:30902870..31007751hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38104882
hg19104882
hg18104882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939267
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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