A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993859



Internal ID21903202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44510748..44510799hg38UCSC Ensembl
chr3:44552240..44552291hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993859
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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