A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843520



Internal ID22027163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108678783..108678783hg38UCSC Ensembl
chr11:108549510..108549510hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258324
Supporting Variants
Samples
Known GenesDDX10
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843520
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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