A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549382



Internal ID21873737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20243140..20269904hg38UCSC Ensembl
chr3:20284632..20311396hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3826765
hg1926765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549382
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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