A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524064



Internal ID22393493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47871866..47871866hg38UCSC Ensembl
chr8:48784427..48784427hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459142
SamplesHG00733
Known GenesPRKDC
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a AluS mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3524064
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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