A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010456



Internal ID6722545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:45568225..45568810hg38UCSC Ensembl
Outerchr3:45609717..45610302hg19UCSC Ensembl
Outerchr3:45584721..45585306hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38586
hg19586
hg18586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv106e180
Supporting Variantsessv3564639
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010456
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