A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995062



Internal ID6731012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41239327..41242693hg38UCSC Ensembl
Innerchr19:41745232..41748598hg19UCSC Ensembl
Innerchr19:46437072..46440438hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383367
hg193367
hg183367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586890
SamplesHuRef
Known GenesAXL
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995062
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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