A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698377



Internal ID21724698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112146052..112146052hg38UCSC Ensembl
chr11:112016775..112016775hg19UCSC Ensembl
Cytoband11q23.1
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 Variantsnssv17191587, nssv17230949
Samples
Known GenesIL18
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)nsv5698377
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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