A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210787



Internal ID22358577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26245073..26256565hg38UCSC Ensembl
Outerchr18:23825037..23836529hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3811493
hg1911493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14262053, nssv14262052
SamplesNA19239, HG00733
Known GenesTAF4B
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210787
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