A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5684015



Internal ID21710336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166062363..166062363hg38UCSC Ensembl
chr6:166475851..166475851hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17180807
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)nsv5684015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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