A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587090



Internal ID7058472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54224577..54240655hg38UCSC Ensembl
Innerchr19:54728449..54744531hg19UCSC Ensembl
Innerchr19:59420261..59436343hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3816079
hg1916083
hg1816083
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006146
Supporting Variants
SamplesHuRef
Known GenesLILRA6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587090
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