A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111554



Internal ID21294820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:31217120..31377401hg38UCSC Ensembl
Innerchr20:29804955..29965204hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38160282
hg19160250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099865
Samplessample158
Known GenesDEFB115, DEFB116, DEFB118, DEFB119
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111554
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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