A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586577



Internal ID16373986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63548764..63588484hg38UCSC Ensembl
Innerchr20:62180117..62219837hg19UCSC Ensembl
Innerchr20:61650561..61690281hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3839721
hg1939721
hg1839721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7668n54
Supporting Variantsnssv943755
Samples
Known GenesC20orf195, GMEB2, HELZ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586577
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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