A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993059



Internal ID21902402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22537360..22581040hg38UCSC Ensembl
chr3:22578851..22622531hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3843681
hg1943681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993059
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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