A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5680982



Internal ID21707303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42974362..42974362hg38UCSC Ensembl
chr4:42976379..42976379hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17209591, nssv17227025
Samples
Known GenesGRXCR1
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)nsv5680982
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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