A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17014272



Internal ID77183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102532604..102580453hg38UCSC Ensembl
chr8:103544832..103592681hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3847850
hg1947850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478977
Supporting Variants
Samples
Known GenesODF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17014272
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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