A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722116



Internal ID145782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19665062..19667504hg38UCSC Ensembl
chr19:19775871..19778313hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382443
hg192443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527356
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722116
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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