A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108328



Internal ID21276410
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 StatusS
Merged Variantsnsv3110911
Supporting Variants
Samplessample236
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108328
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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