A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527066



Internal ID18825347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18639702..19746329hg38UCSC Ensembl
Innerchr14:19416179..20214488hg19UCSC Ensembl
Innerchr14:18486179..19284328hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381106628
hg19798310
hg18798150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037829
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nssv3527066
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