A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5682067



Internal ID21708388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192572402..192572402hg38UCSC Ensembl
chr3:192290191..192290191hg19UCSC Ensembl
Cytoband3q28
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 Variantsnssv17230941
Samples
Known GenesFGF12
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)nsv5682067
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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