A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586060



Internal ID6710756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14621691..14623185hg38UCSC Ensembl
Innerchr19:14732503..14733997hg19UCSC Ensembl
Innerchr19:14593503..14594997hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381495
hg191495
hg181495
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995771
Supporting Variants
SamplesHuRef
Known GenesEMR3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586060
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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