A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586568



Internal ID16027291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63486715..63502196hg38UCSC Ensembl
Innerchr20:62118068..62133549hg19UCSC Ensembl
Innerchr20:61588512..61603993hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3815482
hg1915482
hg1815482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv943748
Samples
Known GenesEEF1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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