A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698662



Internal ID21724983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22063681..22063681hg38UCSC Ensembl
chr12:22216615..22216615hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17192688, nssv17231570
Samples
Known GenesCMAS
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)nsv5698662
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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