A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5685614



Internal ID21711935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45102302..45102302hg38UCSC Ensembl
chr1:45567974..45567974hg19UCSC Ensembl
Cytoband1p34.1
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 Variantsnssv17211003, nssv17206535
Samples
Known GenesZSWIM5
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)nsv5685614
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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