A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221483



Internal ID22365857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:28063112..28089005hg38UCSC Ensembl
Outerchr9:28063110..28089003hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3825894
hg1925894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281642, nssv14281640, nssv14281641
SamplesNA19238, HG00732, HG00733
Known GenesLINGO2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221483
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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