A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9484n152



Internal ID22825187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13424322..13425732hg38UCSC Ensembl
chr9:13424321..13425731hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3190994, nsv3207222
SamplesNA19240, HG00514
Known GenesFLJ41200
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9484n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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