A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586569



Internal ID16027292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63496168..63548764hg38UCSC Ensembl
Innerchr20:62127521..62180117hg19UCSC Ensembl
Innerchr20:61597965..61650561hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3852597
hg1952597
hg1852597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943749
Samples
Known GenesEEF1A2, PPDPF, PTK6, SRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586569
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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