A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5694512



Internal ID21720833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48338679..48338679hg38UCSC Ensembl
chr10:49546722..49546722hg19UCSC Ensembl
Cytoband10q11.22
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 Variantsnssv17188506
Samples
Known GenesMAPK8
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)nsv5694512
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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