A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993053



Internal ID21902396
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 StatusM
Merged Variants
Supporting Variantsnssv17556478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993053
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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