A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933221



Internal ID22876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68568828..68595131hg38UCSC Ensembl
chr3:68617979..68644282hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3826304
hg1926304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933221
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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