A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5679611



Internal ID21705932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60819111..60819111hg38UCSC Ensembl
chr5:60114938..60114938hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17212167
Samples
Known GenesELOVL7
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)nsv5679611
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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