A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5695272



Internal ID21721593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114319024..114319024hg38UCSC Ensembl
chr11:114189746..114189746hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17216577, nssv17191899
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)nsv5695272
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