A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008130



Internal ID7073224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:13261872..13263197hg38UCSC Ensembl
Innerchr18:13261871..13263196hg19UCSC Ensembl
Innerchr18:13251871..13253196hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381326
hg191326
hg181326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586650
SamplesHuRef
Known GenesLDLRAD4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008130
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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