A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015187



Internal ID77778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109104369..109104420hg38UCSC Ensembl
chr8:110116598..110116649hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406173
Supporting Variants
Samples
Known GenesTRHR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015187
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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