A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5706410



Internal ID21732731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48313573..48313573hg38UCSC Ensembl
chr8:49226133..49226133hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17223515, nssv17184655
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)nsv5706410
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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