A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698470



Internal ID21724791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23886277..23886277hg38UCSC Ensembl
chr13:24460416..24460416hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17193433
Samples
Known GenesMIPEP
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)nsv5698470
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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