A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006709



Internal ID6718825
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586867
SamplesHuRef
Known GenesPTPRS
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006709
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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