A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5680337



Internal ID21706658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139874487..139874487hg38UCSC Ensembl
chr3:139593329..139593329hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17208428
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)nsv5680337
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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