A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027786



Internal ID86227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114795483..114795595hg38UCSC Ensembl
chr9:117557763..117557875hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484180
Supporting Variants
Samples
Known GenesTNFSF15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027786
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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