A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1176n100



Internal ID20152792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55584048..55686088hg38UCSC Ensembl
chr11:55351524..55453564hg19UCSC Ensembl
chr11:55108100..55210140hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38102041
hg19102041
hg18102041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035185, nsv1036326, nsv1054079, nsv1039881, nsv1040728, nsv1036845, nsv1048215, nsv1047160
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1176n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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