A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932434



Internal ID22338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33329515..33329564hg38UCSC Ensembl
chr3:33371007..33371056hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543280
Supporting Variants
Samples
Known GenesFBXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932434
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003434


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