A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1053n100



Internal ID22787140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5825846..5866695hg38UCSC Ensembl
chr11:5847076..5887925hg19UCSC Ensembl
chr11:5803652..5844501hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3840850
hg1940850
hg1840850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043316, nsv1042501
Samples
Known GenesOR52E6, OR52E8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1053n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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