A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520425



Internal ID22389833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76850869..76850869hg38UCSC Ensembl
chr17:74846951..74846951hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14418726
SamplesHG00514
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)nsv3520425
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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