A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5681942



Internal ID21708263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4990831..4990831hg38UCSC Ensembl
chr2:5130964..5130964hg19UCSC Ensembl
Cytoband2p25.2
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 Variantsnssv17195462, nssv17205844
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)nsv5681942
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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