A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702490



Internal ID126156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75904493..76030101hg38UCSC Ensembl
chr15:76196834..76322442hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38125609
hg19125609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529979
Supporting Variants
Samples
Known GenesFBXO22, FBXO22-AS1, NRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702490
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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