A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5714161



Internal ID21740482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69461865..69461865hg38UCSC Ensembl
chr15:69754204..69754204hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17198179, nssv17230227
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)nsv5714161
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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