A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586150



Internal ID7057532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39878192..39894697hg38UCSC Ensembl
Innerchr19:40368832..40385337hg19UCSC Ensembl
Innerchr19:45060672..45077177hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3816506
hg1916506
hg1816506
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006063
Supporting Variants
SamplesHuRef
Known GenesFCGBP
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586150
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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