A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995771



Internal ID6731719
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586060
SamplesHuRef
Known GenesEMR3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995771
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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