A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842639



Internal ID22026282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104264183..104264183hg38UCSC Ensembl
chr10:106023941..106023941hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247462
Supporting Variants
Samples
Known GenesGSTO1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842639
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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