A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5687876



Internal ID21714197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188849346..188849346hg38UCSC Ensembl
chr3:188567134..188567134hg19UCSC Ensembl
Cytoband3q28
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 Variantsnssv17225971, nssv17208528
Samples
Known GenesLPP
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)nsv5687876
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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