A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421879



Internal ID200940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114488091..114488142hg38UCSC Ensembl
chr11:114358813..114358864hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421879
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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