A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696657



Internal ID21722978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70627534..70627534hg38UCSC Ensembl
chr15:70919873..70919873hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17227358, nssv17197817
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)nsv5696657
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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