A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991905



Internal ID21901248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170901562..170902615hg38UCSC Ensembl
chr3:170619351..170620404hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556200
Samples
Known GenesEIF5A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991905
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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