A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520460



Internal ID22389868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78310299..78310299hg38UCSC Ensembl
chr10:80070056..80070056hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14415037
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)nsv3520460
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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