A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043978



Internal ID97052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42920260..42920311hg38UCSC Ensembl
chr11:42941810..42941861hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043978
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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