A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842692



Internal ID22026335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19232851..19232851hg38UCSC Ensembl
chr11:19254398..19254398hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247828
Supporting Variants
Samples
Known GenesE2F8
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842692
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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