A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698594



Internal ID21724915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3489369..3489369hg38UCSC Ensembl
chr20:3470016..3470016hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17202784
Samples
Known GenesATRN
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)nsv5698594
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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