A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509126



Internal ID18460721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55695666hg38UCSC Ensembl
Innerchr11:55361349..55463142hg19UCSC Ensembl
Innerchr11:55117925..55219718hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38101794
hg19101794
hg18101794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037738
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509126
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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