A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933157



Internal ID22830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65058738..65078353hg38UCSC Ensembl
chr3:65044413..65064028hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3819616
hg1919616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933157
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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