A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037738



Internal ID18780269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55695666hg38UCSC Ensembl
Innerchr11:55361349..55463142hg19UCSC Ensembl
Innerchr11:55117925..55219718hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38101794
hg19101794
hg18101794
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1178n100
Supporting Variantsnssv3518014, nssv3509126
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037738
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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