A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933679



Internal ID23186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45041403..45041482hg38UCSC Ensembl
chr3:45082895..45082974hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139830
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.018084


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