A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556478



Internal ID21880833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20880300..20885720hg38UCSC Ensembl
chr3:20921792..20927212hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385421
hg195421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556478
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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