A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1179n100



Internal ID20152795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55595852..55695666hg38UCSC Ensembl
chr11:55363328..55463142hg19UCSC Ensembl
chr11:55119904..55219718hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3899815
hg1999815
hg1899815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038036, nsv1039236
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)dgv1179n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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