A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045494



Internal ID18788025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55641874hg38UCSC Ensembl
Innerchr11:55361349..55409350hg19UCSC Ensembl
Innerchr11:55117925..55165926hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3848002
hg1948002
hg1848002
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1177n100
Supporting Variantsnssv3517308, nssv3510349, nssv3514314
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045494
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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