A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5706544



Internal ID21732865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39937490..39937490hg38UCSC Ensembl
chr15:40229691..40229691hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17197462
Samples
Known GenesEIF2AK4
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)nsv5706544
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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