A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995198



Internal ID7079621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:125473217..125474397hg38UCSC Ensembl
Innerchr8:126485459..126486639hg19UCSC Ensembl
Innerchr8:126554641..126555821hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381181
hg191181
hg181181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586878
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995198
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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