A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5690431



Internal ID21716752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167665241..167665241hg38UCSC Ensembl
chr3:167383029..167383029hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17208483, nssv17230780
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)nsv5690431
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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