A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843257



Internal ID22026900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110452062..110452062hg38UCSC Ensembl
chr11:110322786..110322786hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258334
Supporting Variants
Samples
Known GenesFDX1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843257
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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