A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722726



Internal ID146392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30598218..30613878hg38UCSC Ensembl
chr19:31089125..31104785hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3815661
hg1915661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520358
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722726
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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