A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161545



Internal ID7906259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107608636..107685099hg38UCSC Ensembl
Innerchr11:107479362..107555825hg19UCSC Ensembl
Innerchr11:106984572..107061035hg18UCSC Ensembl
Innerchr11:106984572..107061035hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3876464
hg1976464
hg1876464
hg1776464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422201
Supporting Variants
SamplesND05296
Known GenesELMOD1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161545
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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