A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9725n152



Internal ID22825428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113453346..113453538hg38UCSC Ensembl
chr9:116215626..116215818hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3288260, nsv3283869
SamplesNA19240, HG00514
Known GenesRGS3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9725n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer