A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989409



Internal ID7076110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13196791..13208427hg38UCSC Ensembl
Outerchr3:13238291..13249927hg19UCSC Ensembl
Outerchr3:13213291..13224927hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3811637
hg1911637
hg1811637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565287
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989409
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