A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv77e180



Internal ID22757487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54224577..54240655hg38UCSC Ensembl
chr19:54728449..54744531hg19UCSC Ensembl
chr19:59420261..59436343hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3816079
hg1916083
hg1816083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv988540, esv1006146
SamplesHuRef
Known GenesLILRA6
MethodOligo aCGH
SNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv77e180
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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