A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039234



Internal ID93884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114876531..115123609hg38UCSC Ensembl
chr10:116636290..116883373hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38247079
hg19247084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500278
Supporting Variants
Samples
Known GenesATRNL1, FAM160B1, TRUB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039234
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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