A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5678987



Internal ID21705308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2341265..2341265hg38UCSC Ensembl
chr5:2341379..2341379hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17176808
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)nsv5678987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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