A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027701



Internal ID86171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119342100..119342100hg38UCSC Ensembl
chr9:122104378..122104378hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545435
Supporting Variants
Samples
Known GenesBRINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027701
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009701


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