A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9636n152



Internal ID22825339
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 StatusM
Merged Variants
Supporting Variantsnsv3243332, nsv3236456
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9636n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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