A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5702618



Internal ID21728939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37630410..37630410hg38UCSC Ensembl
chr17:35990440..35990440hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17200273
Samples
Known GenesDDX52
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)nsv5702618
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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