A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228208



Internal ID22370470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38895305..38905515hg38UCSC Ensembl
Outerchr22:39291310..39301520hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3810211
hg1910211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14269400, nssv14269401
SamplesHG00731, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228208
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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