A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026395



Internal ID85336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113419448..113419663hg38UCSC Ensembl
chr9:116181728..116181943hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476081
Supporting Variants
Samples
Known GenesC9orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026395
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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