A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5674983



Internal ID21701304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144044398..144044398hg38UCSC Ensembl
chr3:143763240..143763240hg19UCSC Ensembl
Cytoband3q24
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 Variantsnssv17218629
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)nsv5674983
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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