A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020799



Internal ID81512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19103745..19106643hg38UCSC Ensembl
chr9:19103743..19106641hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg382899
hg192899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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