A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053368



Internal ID103427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123375688..123375739hg38UCSC Ensembl
chr11:123246396..123246447hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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