A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930452



Internal ID21045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30943648..30943702hg38UCSC Ensembl
chr3:30985140..30985194hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930452
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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