A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054041



Internal ID19143260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19637241..19952068hg38UCSC Ensembl
Innerchr14:20105479..20420227hg19UCSC Ensembl
Innerchr14:19175240..19490067hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38314828
hg19314749
hg18314828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1775n100
Supporting Variantsnssv3527477, nssv3527476, nssv3711196, nssv3527483, nssv3527487, nssv3527485, nssv3527484, nssv3527482, nssv3527478, nssv3527475, nssv3527486, nssv3711203, nssv3711201, nssv3527480, nssv3527481, nssv3711199, nssv3711202, nssv3527479, nssv3711200, nssv3711197, nssv3711198
Samples
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054041
Frequency
Sample Size11257
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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