A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002091



Internal ID6714226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54626506..54627738hg38UCSC Ensembl
Innerchr1:55092179..55093411hg19UCSC Ensembl
Innerchr1:54864767..54865999hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381233
hg191233
hg181233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586810
SamplesHuRef
Known GenesACOT11
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002091
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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