A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007881



Internal ID7072974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89829955..89831994hg38UCSC Ensembl
Innerchr16:89896363..89898402hg19UCSC Ensembl
Innerchr16:88423864..88425903hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382040
hg192040
hg182040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63e180
Supporting Variantsessv3586367
SamplesHuRef
Known GenesSPIRE2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007881
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