A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041043



Internal ID19130262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18676837..19926956hg38UCSC Ensembl
Innerchr14:19453314..20395115hg19UCSC Ensembl
Innerchr14:18523314..19464955hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381250120
hg19941802
hg18941642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n100
Supporting Variantsnssv3528094
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041043
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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