A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3538n152



Internal ID22819241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36187407..36460604hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38273198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3227172, nsv3217301
SamplesNA19238, NA19239, HG00732, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv3538n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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