A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211128



Internal ID22358792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126757104..126762851hg38UCSC Ensembl
Outerchr9:129519383..129525130hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385748
hg195748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283673, nssv14283672
SamplesHG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211128
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