A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1056n100



Internal ID20152672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6733555..6877383hg38UCSC Ensembl
chr11:6754786..6898614hg19UCSC Ensembl
chr11:6711362..6855190hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38143829
hg19143829
hg18143829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048857, nsv1039455, nsv1053167
Samples
Known GenesOR10A2, OR10A4, OR10A5, OR2AG1, OR2AG2, OR6A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1056n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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