A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229632



Internal ID22371422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:18928220..18936018hg38UCSC Ensembl
Outerchr22:18915733..18923531hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg387799
hg197799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14269319
SamplesNA19239
Known GenesPRODH
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229632
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