A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706408



Internal ID19004689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4784692..4886442hg38UCSC Ensembl
Innerchr11:4805922..4907672hg19UCSC Ensembl
Innerchr11:4762498..4864248hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38101751
hg19101751
hg18101751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035355
Supporting Variants
Samples
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706408
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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