A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983190



Internal ID12628277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55068148..56083548hg38UCSC Ensembl
Innerchr11:54835624..55851024hg19UCSC Ensembl
Innerchr11:54592200..55607600hg18UCSC Ensembl
Innerchr11:54592200..55607600hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg381015401
hg191015401
hg181015401
hg171015401
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, OR5AS1, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5L1, OR5L2, OR5W2, OR7E5P, TRIM48, TRIM51, TRIM51HP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983190
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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