A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988798



Internal ID6724768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6907939..6908499hg38UCSC Ensembl
Innerchr16:6957940..6958500hg19UCSC Ensembl
Innerchr16:6897941..6898501hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38561
hg19561
hg18561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586614
SamplesHuRef
Known GenesRBFOX1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988798
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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