A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5701436



Internal ID21727757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38509105..38509105hg38UCSC Ensembl
chr15:38801306..38801306hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17197431, nssv17220817
Samples
Known GenesRASGRP1
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)nsv5701436
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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