A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5698362



Internal ID21724683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102047753..102047753hg38UCSC Ensembl
chr12:102441531..102441531hg19UCSC Ensembl
Cytoband12q23.2
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 Variantsnssv17193307
Samples
Known GenesCCDC53
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)nsv5698362
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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