A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5682295



Internal ID21708616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75736514..75736514hg38UCSC Ensembl
chr1:76202199..76202199hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17225506
Samples
Known GenesACADM
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)nsv5682295
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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