A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053972



Internal ID19143191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19424960..19956767hg38UCSC Ensembl
Innerchr14:20010901..20424926hg19UCSC Ensembl
Innerchr14:19080901..19494766hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38531808
hg19414026
hg18413866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1772n100
Supporting Variantsnssv3527442, nssv3527438, nssv3527437, nssv3527441, nssv3527439, nssv3527440
Samples
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053972
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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