A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113924



Internal ID21297190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:69611843..69623118hg38UCSC Ensembl
Innerchr4:70477561..70488836hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3811276
hg1911276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092204
Samplessample231
Known GenesUGT2A1, UGT2A2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113924
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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