A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1051n100



Internal ID22787138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5766838..5797091hg38UCSC Ensembl
chr11:5788068..5818321hg19UCSC Ensembl
chr11:5744644..5774897hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3830254
hg1930254
hg1830254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043847, nsv1041139
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1051n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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