A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3522619



Internal ID22392041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125011861..125011861hg38UCSC Ensembl
chr8:126024103..126024103hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14429663, nssv14455087, nssv14402384
SamplesNA19240, HG00733, HG00514
Known GenesSQLE
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)nsv3522619
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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