A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1164n100



Internal ID20152780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54953335..55445805hg38UCSC Ensembl
chr11:54720811..55213281hg19UCSC Ensembl
chr11:54477387..54969857hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38492471
hg19492471
hg18492471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048402, nsv1038336, nsv1042875, nsv1039155
Samples
Known GenesOR4A15, OR4A16, 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)dgv1164n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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