A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993285



Internal ID21902628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21378282..21382941hg38UCSC Ensembl
chr3:21419774..21424433hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384660
hg194660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993285
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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