A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993373



Internal ID21902716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4084855..4203810hg38UCSC Ensembl
chr3:4126539..4245494hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38118956
hg19118956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993373
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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