A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5694811



Internal ID21721132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36899366..36899366hg38UCSC Ensembl
chr15:37191567..37191567hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17197730
Samples
Known GenesMEIS2
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)nsv5694811
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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