A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524627



Internal ID22394062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87613909..87613909hg38UCSC Ensembl
chr10:89373666..89373666hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392010
SamplesNA19240
Known Genes
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)nsv3524627
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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