A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17189466



Internal ID21636975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8051349..8051349hg38UCSC Ensembl
chr11:8072896..8072896hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5698699
Supporting Variants
Samples
Known GenesTUB
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)nssv17189466
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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