A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5699282



Internal ID21725603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17580799..17580799hg38UCSC Ensembl
chr17:17484113..17484113hg19UCSC Ensembl
Cytoband17p11.2
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 Variantsnssv17222033, nssv17200226
Samples
Known GenesPEMT
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)nsv5699282
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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