A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5674617



Internal ID21700938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39476696..39476696hg38UCSC Ensembl
chr2:39703837..39703837hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17201239, nssv17207864
Samples
Known GenesLOC728730
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)nsv5674617
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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