A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1166n100



Internal ID22787253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55006405..55595852hg38UCSC Ensembl
chr11:54773881..55363328hg19UCSC Ensembl
chr11:54530457..55119904hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38589448
hg19589448
hg18589448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051643, nsv1053949
Samples
Known GenesOR4A15, OR4A16, OR4C15, OR4C16, TRIM48, TRIM51HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1166n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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