A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586619



Internal ID7058001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66630955..66631599hg38UCSC Ensembl
Innerchr9:65968361..65969005hg19UCSC Ensembl
Innerchr9:65708181..65708825hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38645
hg19645
hg18645
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv987820
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586619
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