A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5681228



Internal ID21707549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64516389..64516389hg38UCSC Ensembl
chr5:63812216..63812216hg19UCSC Ensembl
Cytoband5q12.3
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 Variantsnssv17177728
Samples
Known GenesRGS7BP
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)nsv5681228
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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