A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110911



Internal ID21294177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20898..162098hg38UCSC Ensembl
Innerchr3:62576..203781hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38141201
hg19141206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108328
Samplessample236
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110911
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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