A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039293



Internal ID93918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115625502..115630991hg38UCSC Ensembl
chr10:117385012..117390501hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385490
hg195490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510813
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039293
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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