A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225622



Internal ID22368697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:22983556..23006988hg38UCSC Ensembl
Outerchr9:22983555..23006987hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3823433
hg1923433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281634
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225622
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