A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5693052



Internal ID21719373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165233533..165233533hg38UCSC Ensembl
chr5:164660539..164660539hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17179315
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)nsv5693052
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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