A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5707373



Internal ID21733694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119009452..119009452hg38UCSC Ensembl
chr11:118880162..118880162hg19UCSC Ensembl
Cytoband11q23.3
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 Variantsnssv17190661, nssv17216694
Samples
Known GenesCCDC84
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)nsv5707373
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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