A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722586



Internal ID146252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28402739..28402813hg38UCSC Ensembl
chr19:28893646..28893720hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525928
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722586
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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