A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563880



Internal ID7034980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26182326..26186216hg38UCSC Ensembl
Outerchr18:23762290..23766180hg19UCSC Ensembl
Outerchr18:22016288..22020178hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383891
hg193891
hg183891
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995923
Supporting Variants
SamplesHuRef
Known GenesPSMA8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563880
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