A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043063



Internal ID96416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29497317..29497368hg38UCSC Ensembl
chr11:29518864..29518915hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043063
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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