A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9552n152



Internal ID22825255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40514133..40614719hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38100587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3218380, nsv3229144
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9552n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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