A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3521167



Internal ID22390580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109499103..109499103hg38UCSC Ensembl
chr9:112261383..112261383hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14404205
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)nsv3521167
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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