A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5683762



Internal ID21710083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94704584..94704584hg38UCSC Ensembl
chr5:94040289..94040289hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17213133, nssv17178072
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)nsv5683762
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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