A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224984



Internal ID22368254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:96604327..96610431hg38UCSC Ensembl
Outerchr9:99366609..99372713hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386105
hg196105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281974
SamplesNA19240
Known GenesCDC14B
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224984
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer