A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3523092



Internal ID22392517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23853966..23853966hg38UCSC Ensembl
chr16:23865287..23865287hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14419323
SamplesHG00514
Known GenesPRKCB
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)nsv3523092
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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