A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520048



Internal ID22389456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9950380..9950380hg38UCSC Ensembl
chr8:9807890..9807890hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459942, nssv14401661, nssv14428570
SamplesNA19240, HG00733, HG00514
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)nsv3520048
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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