A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724334



Internal ID148000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57337360..57339584hg38UCSC Ensembl
chr19:57848728..57850952hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382225
hg192225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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