A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992386



Internal ID21901729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179638472..179639546hg38UCSC Ensembl
chr3:179356260..179357334hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992386
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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