A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007212



Internal ID6719326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61855390..62087447hg38UCSC Ensembl
Innerchr9:44991542..45223599hg19UCSC Ensembl
Innerchr9:44931538..45163595hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38232058
hg19232058
hg18232058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586051
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007212
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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