A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586515



Internal ID6711211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25340823..25342571hg38UCSC Ensembl
Innerchr2:25563692..25565440hg19UCSC Ensembl
Innerchr2:25417196..25418944hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381749
hg191749
hg181749
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988737
Supporting Variants
SamplesHuRef
Known GenesDNMT3A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586515
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