A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5687901



Internal ID21714222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98848428..98848428hg38UCSC Ensembl
chr5:98184132..98184132hg19UCSC Ensembl
Cytoband5q15
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 Variantsnssv17176622
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)nsv5687901
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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