A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210321



Internal ID22358258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26342543..26353604hg38UCSC Ensembl
Outerchr6:26342771..26353832hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3811062
hg1911062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7789n152
Supporting Variantsnssv14276109, nssv14276108
SamplesNA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210321
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