A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042927



Internal ID19132146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19799717..19957689hg38UCSC Ensembl
Innerchr14:20267876..20425848hg19UCSC Ensembl
Innerchr14:19337716..19495688hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38157973
hg19157973
hg18157973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1787n100
Supporting Variantsnssv3712107
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042927
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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