A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026379



Internal ID85327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113340934..113340937hg38UCSC Ensembl
chr9:116103214..116103217hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026379
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.023572


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