A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046927



Internal ID18789458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55595852..55674830hg38UCSC Ensembl
Innerchr11:55363328..55442306hg19UCSC Ensembl
Innerchr11:55119904..55198882hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3878979
hg1978979
hg1878979
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1178n100
Supporting Variantsnssv3507699, nssv3506749, nssv3709080, nssv3516023, nssv3511719, nssv3516731, nssv3709081, nssv3504308
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)nsv1046927
Frequency
Sample Size29084
Observed Gain2
Observed Loss6
Observed Complex0
Frequencyn/a


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