A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5705555



Internal ID21731876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78817707..78817707hg38UCSC Ensembl
chr15:79110049..79110049hg19UCSC Ensembl
Cytoband15q25.1
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 Variantsnssv17228197, nssv17197587
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)nsv5705555
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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