A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17219588



Internal ID21667097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52212355..52212355hg38UCSC Ensembl
chr16:52246267..52246267hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5697748
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)nssv17219588
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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