A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720593



Internal ID144259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3560367..3569484hg38UCSC Ensembl
chr19:3560365..3569482hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389118
hg199118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720593
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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