A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028245



Internal ID86525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107318967..107321727hg38UCSC Ensembl
chr9:110081248..110084008hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382761
hg192761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478525
Supporting Variants
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028245
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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