A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044066



Internal ID18786597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55591972..55663576hg38UCSC Ensembl
Innerchr11:55359448..55431052hg19UCSC Ensembl
Innerchr11:55116024..55187628hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3871605
hg1971605
hg1871605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1173n100
Supporting Variantsnssv3712397, nssv3509201
Samples
Known GenesOR4C11, 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)nsv1044066
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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