A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463676



Internal ID22228844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86586769..86589304hg38UCSC Ensembl
chr9:89201684..89204219hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382536
hg192536
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236456
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion variant involving LTR satellite DNA
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14463676
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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