A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997129



Internal ID6733071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62123966..62125002hg38UCSC Ensembl
Innerchr11:61891438..61892474hg19UCSC Ensembl
Innerchr11:61648014..61649050hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381037
hg191037
hg181037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587151
SamplesHuRef
Known GenesINCENP
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997129
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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