A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5711215



Internal ID21737536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16576746..16576746hg38UCSC Ensembl
chr20:16557391..16557391hg19UCSC Ensembl
Cytoband20p12.1
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 Variantsnssv17203138
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)nsv5711215
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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