A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5710606



Internal ID21736927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131826970..131826970hg38UCSC Ensembl
chr8:132839217..132839217hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17185625, nssv17217034
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)nsv5710606
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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