A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986364



Internal ID12628271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55072848..56026048hg38UCSC Ensembl
Innerchr11:54840324..55793524hg19UCSC Ensembl
Innerchr11:54596900..55550100hg18UCSC Ensembl
Innerchr11:54596900..55550100hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38953201
hg19953201
hg18953201
hg17953201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751030
Supporting Variants
SamplesBEC_552
Known GenesOR10AG1, OR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5L1, OR5L2, OR5W2, OR7E5P, TRIM48, TRIM51, TRIM51HP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986364
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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