A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5697602



Internal ID21723923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65444829..65444829hg38UCSC Ensembl
chr15:65737167..65737167hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17198129
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)nsv5697602
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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