A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5696100



Internal ID21722421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70724986..70724986hg38UCSC Ensembl
chr13:71299118..71299118hg19UCSC Ensembl
Cytoband13q21.33
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 Variantsnssv17228418, nssv17195534
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)nsv5696100
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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