A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039190



Internal ID93859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114130862..114130913hg38UCSC Ensembl
chr10:115890621..115890672hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5398821
Supporting Variants
Samples
Known GenesC10orf118
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039190
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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