A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5683889



Internal ID21710210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92191050..92191050hg38UCSC Ensembl
chr6:92900768..92900768hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17178503
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)nsv5683889
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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