A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5711082



Internal ID21737403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87682098..87682098hg38UCSC Ensembl
chr15:88225329..88225329hg19UCSC Ensembl
Cytoband15q25.3
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 Variantsnssv17197886, nssv17224659
Samples
Known Genes
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)nsv5711082
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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