A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1204n100



Internal ID22787291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55654851..55865297hg38UCSC Ensembl
chr11:55422327..55632773hg19UCSC Ensembl
chr11:55178903..55389349hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38210447
hg19210447
hg18210447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037568, nsv1035956, nsv1053068, nsv1048912, nsv1050001, nsv1045642, nsv1040617, nsv1052431, nsv1049992, nsv1040041, nsv1048776, nsv1053172, nsv1048634, nsv1052294, nsv1037538, nsv1040373, nsv1037184, nsv1040984, nsv1042841, nsv1045667, nsv1043315, nsv1052597, nsv1048654
Samples
Known GenesOR4C6, OR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1204n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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