A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5680207



Internal ID21706528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157483378..157483378hg38UCSC Ensembl
chr2:158339890..158339890hg19UCSC Ensembl
Cytoband2q24.1
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 Variantsnssv17209297, nssv17225740
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)nsv5680207
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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