A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006711



Internal ID7071803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12169846..12177453hg38UCSC Ensembl
Innerchr8:12027355..12034962hg19UCSC Ensembl
Innerchr8:12064764..12072371hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg387608
hg197608
hg187608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586207
SamplesHuRef
Known GenesFAM90A2P
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006711
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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