A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429415



Internal ID22171104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86586767..86589312hg38UCSC Ensembl
chr9:89201682..89204227hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382546
hg192546
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243332
Supporting Variants
SamplesHG00514
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)nssv14429415
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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