A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5705592



Internal ID21731913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:126018412..126018412hg38UCSC Ensembl
chr12:126502958..126502958hg19UCSC Ensembl
Cytoband12q24.32
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 Variantsnssv17216501, nssv17194282
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)nsv5705592
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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