A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1026n100



Internal ID22787113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4784692..4889142hg38UCSC Ensembl
chr11:4805922..4910372hg19UCSC Ensembl
chr11:4762498..4866948hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38104451
hg19104451
hg18104451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035355, nsv1039703
Samples
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1026n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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