A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5675090



Internal ID21701411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181778156..181778156hg38UCSC Ensembl
chr3:181495944..181495944hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17211545
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)nsv5675090
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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