A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023634



Internal ID83468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34192728..34197802hg38UCSC Ensembl
chr9:34192726..34197800hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg385075
hg195075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484486
Supporting Variants
Samples
Known GenesUBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023634
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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