A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113886



Internal ID21297152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107430188..107432983hg38UCSC Ensembl
Innerchr3:107149035..107151830hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382796
hg192796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107850
Samplessample289
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113886
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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