A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5697416



Internal ID21723737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131756212..131756212hg38UCSC Ensembl
chr12:132240757..132240757hg19UCSC Ensembl
Cytoband12q24.33
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 Variantsnssv17194024, nssv17218808
Samples
Known GenesSFSWAP
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)nsv5697416
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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