A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5699811



Internal ID21726132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110334933..110334933hg38UCSC Ensembl
chr11:110205658..110205658hg19UCSC Ensembl
Cytoband11q22.3
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 Variantsnssv17227411, nssv17191556
Samples
Known Genes
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nsv5699811
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer