A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979838



Internal ID12980845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55677818..55827605hg38UCSC Ensembl
Innerchr11:55445294..55595081hg19UCSC Ensembl
Innerchr11:55201870..55351657hg18UCSC Ensembl
Innerchr11:55201870..55351657hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38149788
hg19149788
hg18149788
hg17149788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34561
Supporting Variants
SamplesNA18852
Known GenesOR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979838
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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