A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050052



Internal ID101265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95271667..95271717hg38UCSC Ensembl
chr11:95004831..95004881hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050052
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001249


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