A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063864



Internal ID18806395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33414827..33558912hg38UCSC Ensembl
Innerchr20:32002633..32146718hg19UCSC Ensembl
Innerchr20:31466294..31610379hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38144086
hg19144086
hg18144086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4302n100
Supporting Variantsnssv3584742
Samples
Known GenesCBFA2T2, SNTA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063864
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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