A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044485



Internal ID18787016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55584048..55667639hg38UCSC Ensembl
Innerchr11:55351524..55435115hg19UCSC Ensembl
Innerchr11:55108100..55191691hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3883592
hg1983592
hg1883592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1173n100
Supporting Variantsnssv3510387, nssv3519553
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)nsv1044485
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer