A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842771



Internal ID22026414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69420318..69420318hg38UCSC Ensembl
chr11:69235086..69235086hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842771
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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