A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586221



Internal ID16373630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53775851..53802448hg38UCSC Ensembl
Innerchr20:52392390..52418987hg19UCSC Ensembl
Innerchr20:51825797..51852394hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3826598
hg1926598
hg1826598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941218
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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