A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586211



Internal ID16373620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53667312..53674549hg38UCSC Ensembl
Innerchr20:52283851..52291088hg19UCSC Ensembl
Innerchr20:51717258..51724495hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387238
hg197238
hg187238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7603n54
Supporting Variantsnssv941157
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586211
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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