A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036981



Internal ID18779512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55593873..55678457hg38UCSC Ensembl
Innerchr11:55361349..55445933hg19UCSC Ensembl
Innerchr11:55117925..55202509hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3884585
hg1984585
hg1884585
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1178n100
Supporting Variantsnssv3505944, nssv3510662
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)nsv1036981
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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