A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993453



Internal ID21902796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4037014..4059232hg38UCSC Ensembl
chr3:4078698..4100916hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3822219
hg1922219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993453
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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