A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842760



Internal ID22026403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66778112..66778112hg38UCSC Ensembl
chr11:66545583..66545583hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248156
Supporting Variants
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842760
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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