A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518330



Internal ID18816611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55918323..56051406hg38UCSC Ensembl
Innerchr11:55685799..55818882hg19UCSC Ensembl
Innerchr11:55442375..55575458hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38133084
hg19133084
hg18133084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048664
Supporting Variants
Samples
Known GenesOR10AG1, OR5AS1, OR5F1, OR5I1, OR7E5P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518330
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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