A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026799



Internal ID85589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110244351..110244376hg38UCSC Ensembl
chr9:113006631..113006656hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542491
Supporting Variants
Samples
Known GenesTXN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002822


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