A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17219026



Internal ID21666535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52313728..52313728hg38UCSC Ensembl
chr14:52780446..52780446hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5701257
Supporting Variants
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)nssv17219026
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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