A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161509



Internal ID8252917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101347186..101593917hg38UCSC Ensembl
Innerchr15:101887391..102134120hg19UCSC Ensembl
Innerchr15:99704914..99951643hg18UCSC Ensembl
Innerchr15:99704914..99951643hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38246732
hg19246730
hg18246730
hg17246730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422359
Supporting Variants
SamplesND04845
Known GenesPCSK6
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161509
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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