A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022267



Internal ID82514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11717372..11925282hg38UCSC Ensembl
chr9:11717372..11925282hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38207911
hg19207911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022267
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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