A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722661



Internal ID146327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29566896..29567612hg38UCSC Ensembl
chr19:30057803..30058519hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722661
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.027153


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