A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5699553



Internal ID21725874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91308564..91308564hg38UCSC Ensembl
chr15:91851794..91851794hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17218784, nssv17197929
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)nsv5699553
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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