A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527312



Internal ID18825593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19954095hg38UCSC Ensembl
Innerchr14:19802529..20422254hg19UCSC Ensembl
Innerchr14:18872529..19492094hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38723147
hg19619726
hg18619566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039252
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nssv3527312
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