A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116655



Internal ID21299921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104540452..104570756hg38UCSC Ensembl
Innerchr13:105192803..105223107hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3830305
hg1930305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094361
Samplessample34
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116655
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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