A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702453



Internal ID21728774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69880563..69880563hg38UCSC Ensembl
chr15:70172902..70172902hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17197806
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)nsv5702453
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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