A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983902



Internal ID12977358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54555644..54914139hg38UCSC Ensembl
Innerchr11:51205141..51563636hg19UCSC Ensembl
Innerchr11:51061717..51420212hg18UCSC Ensembl
Innerchr11:51061717..51420212hg17UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38358496
hg19358496
hg18358496
hg17358496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751029
Supporting Variants
SamplesBEC_730
Known GenesOR4A5, OR4C46
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983902
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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