A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9645n152



Internal ID22825348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87856207..87883038hg38UCSC Ensembl
chr9:90471122..90497953hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3826832
hg1926832
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3232773, nsv3232078
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, HG00513
Known GenesLOC392364, SPATA31E1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9645n152
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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