A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422503



Internal ID8253286
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 StatusM
Merged Variants
Supporting Variantsessv5161320
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)esv2422503
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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