A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990133



Internal ID7061376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:114135065..114135776hg38UCSC Ensembl
Outerchr3:113853912..113854623hg19UCSC Ensembl
Outerchr3:115336602..115337313hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38712
hg19712
hg18712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565482
SamplesHuRef
Known GenesDRD3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990133
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