A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161320



Internal ID8252904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5066062..5104761hg38UCSC Ensembl
Innerchr11:5087292..5125991hg19UCSC Ensembl
Innerchr11:5043868..5082567hg18UCSC Ensembl
Innerchr11:5043868..5082567hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3838700
hg1938700
hg1838700
hg1738700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422503
Supporting Variants
SamplesND04531
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161320
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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