A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5712059



Internal ID21738380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45513545..45513545hg38UCSC Ensembl
chr20:44142185..44142185hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17200948
Samples
Known GenesSPINT3
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)nsv5712059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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