A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051199



Internal ID18793730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55307493..55494429hg38UCSC Ensembl
Innerchr11:55074969..55261905hg19UCSC Ensembl
Innerchr11:54831545..55018481hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38186937
hg19186937
hg18186937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504408, nssv3515082
Samples
Known GenesOR4A15, OR4A16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051199
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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