A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520680



Internal ID22390088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51247056..51247056hg38UCSC Ensembl
chr12:51640840..51640840hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383964
SamplesNA19240
Known GenesSMAGP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a AluY mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3520680
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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