A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688374



Internal ID112040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43169780..43169780hg38UCSC Ensembl
chr11:43191330..43191330hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688374
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.290998


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