A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5699624



Internal ID21725945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140299211..140299211hg38UCSC Ensembl
chr8:141309310..141309310hg19UCSC Ensembl
Cytoband8q24.3
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 Variantsnssv17223667
Samples
Known GenesTRAPPC9
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)nsv5699624
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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