A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026233



Internal ID85228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111100732..111137163hg38UCSC Ensembl
chr9:113863012..113899443hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3836432
hg1936432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491272
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026233
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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