A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9640n152



Internal ID22825343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86999015..87001447hg38UCSC Ensembl
chr9:89613930..89616362hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382433
hg192433
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3249404, nsv3239195
SamplesNA19240, HG00514
Known GenesLOC100506834
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9640n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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