A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484180



Internal ID261600
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 StatusM
Merged Variants
Supporting Variantsnssv17027786
Samples
Known GenesTNFSF15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484180
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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