A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5682561



Internal ID21708882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81676318..81676318hg38UCSC Ensembl
chr6:82386035..82386035hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17178484
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)nsv5682561
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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