A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5693686



Internal ID21720007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17114639..17114639hg38UCSC Ensembl
chr1:17441134..17441134hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17205663, nssv17177636
Samples
Known GenesPADI2
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)nsv5693686
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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