A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5711976



Internal ID21738297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58277589..58277589hg38UCSC Ensembl
chr16:58311493..58311493hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17198828
Samples
Known GenesCCDC113
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)nsv5711976
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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