A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979860



Internal ID12980883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55693348..55822848hg38UCSC Ensembl
Innerchr11:55460824..55590324hg19UCSC Ensembl
Innerchr11:55217400..55346900hg18UCSC Ensembl
Innerchr11:55217400..55346900hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38129501
hg19129501
hg18129501
hg17129501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34760
Supporting Variants
SamplesNA18854
Known GenesOR5D13, OR5D14, OR5D18, OR5L1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979860
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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