A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586798



Internal ID6711494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75478640..75479150hg38UCSC Ensembl
Innerchr16:75512538..75513048hg19UCSC Ensembl
Innerchr16:74070039..74070549hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38511
hg19511
hg18511
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007873
Supporting Variants
SamplesHuRef
Known GenesCHST6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586798
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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