A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586867



Internal ID6711563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5208591..5210164hg38UCSC Ensembl
Innerchr19:5208602..5210175hg19UCSC Ensembl
Innerchr19:5159602..5161175hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381574
hg191574
hg181574
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006709
Supporting Variants
SamplesHuRef
Known GenesPTPRS
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586867
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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