A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522326



Internal ID18820607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55918323..56061980hg38UCSC Ensembl
Innerchr11:55685799..55829456hg19UCSC Ensembl
Innerchr11:55442375..55586032hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38143658
hg19143658
hg18143658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053326
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)nssv3522326
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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