A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247462



Internal ID22052072
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 StatusM
Merged Variants
Supporting Variantsnssv17842639
Samples
Known GenesGSTO1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247462
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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