A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842993



Internal ID22026636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110889521..110889521hg38UCSC Ensembl
chr10:112649279..112649279hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247520
Supporting Variants
Samples
Known GenesPDCD4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842993
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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