A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586602



Internal ID7057984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5495967..5497709hg38UCSC Ensembl
Innerchr5:5496080..5497822hg19UCSC Ensembl
Innerchr5:5549080..5550822hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381743
hg191743
hg181743
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995745
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586602
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer