A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3521387



Internal ID22390800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75902323..75902323hg38UCSC Ensembl
chr2:76129449..76129449hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14394143
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)nsv3521387
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer