A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039801



Internal ID94257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98019658..98021951hg38UCSC Ensembl
chr10:99779415..99781708hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382294
hg192294
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562716
Supporting Variants
Samples
Known GenesCRTAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039801
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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