A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007286



Internal ID6719399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76496118..76501251hg38UCSC Ensembl
Innerchr10:78255876..78261009hg19UCSC Ensembl
Innerchr10:77925882..77931015hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385134
hg195134
hg185134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586509
SamplesHuRef
Known GenesC10orf11
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007286
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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