A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054368



Internal ID19143587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19956767hg38UCSC Ensembl
Innerchr14:20200171..20424926hg19UCSC Ensembl
Innerchr14:19270011..19494766hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38224756
hg19224756
hg18224756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3530630, nssv3530619, nssv3530622, nssv3530620, nssv3530627, nssv3530629, nssv3530623, nssv3530624, nssv3530625, nssv3530626, nssv3530621, nssv3530628
Samples
Known GenesOR4K1, 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)nsv1054368
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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