A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215260



Internal ID22361654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:22085500..22117511hg38UCSC Ensembl
Outerchr9:22085499..22117510hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3832012
hg1932012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281968
SamplesNA19240
Known GenesCDKN2B-AS1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215260
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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