A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3522264



Internal ID22391684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4183709..4183709hg38UCSC Ensembl
chr10:4225901..4225901hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380846
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)nsv3522264
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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