A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980552



Internal ID12982621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55677848..55827648hg38UCSC Ensembl
Innerchr11:55445324..55595124hg19UCSC Ensembl
Innerchr11:55201900..55351700hg18UCSC Ensembl
Innerchr11:55201900..55351700hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38149801
hg19149801
hg18149801
hg17149801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35147
Supporting Variants
SamplesNA19209
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)essv6980552
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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