A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9862n152



Internal ID22825565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138226416..138253879hg38UCSC Ensembl
chr9:141116866..141144329hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3827464
hg1927464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3227885, nsv3222062
SamplesNA19239, NA19240
Known GenesFAM157B
MethodMerging
Optical mapping
AnalysisBioNano Genomics proprietary analysis
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformBioNano Genomics
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9862n152
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