A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991595



Internal ID6727559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12041735..12043456hg38UCSC Ensembl
Innerchr17:11945052..11946773hg19UCSC Ensembl
Innerchr17:11885777..11887498hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381722
hg191722
hg181722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586933
SamplesHuRef
Known GenesMAP2K4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991595
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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