A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005795



Internal ID7070889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:125953618..125958052hg38UCSC Ensembl
Innerchr3:125672461..125676895hg19UCSC Ensembl
Innerchr3:127155151..127159585hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg384435
hg194435
hg184435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586723
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005795
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