A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212895



Internal ID22360007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:122483496..122512803hg38UCSC Ensembl
Outerchr9:125245775..125275082hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3829308
hg1929308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281296
SamplesNA19238
Known GenesOR1J2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212895
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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