A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043884



Internal ID96989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41459654..41459687hg38UCSC Ensembl
chr11:41481204..41481237hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559548
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043884
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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