A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1905n54



Internal ID20135329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55267935..56096685hg38UCSC Ensembl
chr11:55035411..55864161hg19UCSC Ensembl
chr11:54791987..55620737hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38828751
hg19828751
hg18828751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554800, nsv554797
Samples
Known GenesOR10AG1, OR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, OR5AS1, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5L1, OR5L2, OR5W2, OR7E5P, OR8I2, TRIM48, TRIM51, TRIM51HP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1905n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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