A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5690979



Internal ID21717300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161249411..161249411hg38UCSC Ensembl
chr2:162105922..162105922hg19UCSC Ensembl
Cytoband2q24.2
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 Variantsnssv17221506
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)nsv5690979
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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