A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3521594



Internal ID22391010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75091476..75091476hg38UCSC Ensembl
chr1:75557160..75557160hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14388422
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)nsv3521594
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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