A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035639



Internal ID91507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68876758..68876809hg38UCSC Ensembl
chr10:70636514..70636565hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5404035
Supporting Variants
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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