A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455087



Internal ID22249569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125011861..125011861hg38UCSC Ensembl
chr8:126024103..126024103hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3522619
Supporting Variants
SamplesHG00733
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)nssv14455087
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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