A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933360



Internal ID22975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49545406..49546536hg38UCSC Ensembl
chr3:49582839..49583969hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933360
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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