A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422339



Internal ID8253122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24983071..25525119hg38UCSC Ensembl
Innerchr11:25004617..25546665hg19UCSC Ensembl
Innerchr11:24961193..25503241hg18UCSC Ensembl
Innerchr11:24961193..25503241hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38542049
hg19542049
hg18542049
hg17542049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161327
SamplesND05155
Known GenesLUZP2
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422339
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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