A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5705169



Internal ID21731490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15502096..15502096hg38UCSC Ensembl
chr11:15523642..15523642hg19UCSC Ensembl
Cytoband11p15.2
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 Variantsnssv17190381, nssv17226404
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)nsv5705169
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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