A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526834



Internal ID18478429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19169707hg38UCSC Ensembl
Innerchr14:19002112..19796172hg19UCSC Ensembl
Innerchr14:18072112..18866172hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38944073
hg19794061
hg18794061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047368
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526834
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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