A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217926



Internal ID22363437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65899143..66021230hg38UCSC Ensembl
Outerchr9:42500110..42613945hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38122088
hg19113836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282855, nssv14282854
SamplesHG00732, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217926
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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