A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842394



Internal ID22026037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43400131..43400131hg38UCSC Ensembl
chr11:43421681..43421681hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248035
Supporting Variants
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842394
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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