A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5704079



Internal ID21730400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2496024..2496024hg38UCSC Ensembl
chr16:2546025..2546025hg19UCSC Ensembl
Cytoband16p13.3
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 Variantsnssv17198272
Samples
Known GenesTBC1D24
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)nsv5704079
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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