A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17019101



Internal ID80363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14521599..14522327hg38UCSC Ensembl
chr9:14521597..14522325hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17019101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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