A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049013



Internal ID19138232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..18693031hg38UCSC Ensembl
Innerchr14:19002112..19469508hg19UCSC Ensembl
Innerchr14:18072112..18539508hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38467397
hg19467397
hg18467397
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525682, nssv3525671, nssv3525683, nssv3525675, nssv3525687, nssv3713329, nssv3525692, nssv3525689, nssv3525684, nssv3525688, nssv3525686, nssv3525673, nssv3525695, nssv3525690, nssv3525680, nssv3525674, nssv3525681, nssv3525677, nssv3525693, nssv3525691, nssv3525679, nssv3525678, nssv3525694, nssv3525676, nssv3525672, nssv3525685, nssv3713330, nssv3713328, nssv3713331, nssv3713332
Samples
Known GenesLOC642426, OR11H12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049013
Frequency
Sample Size11257
Observed Gain28
Observed Loss2
Observed Complex0
Frequencyn/a


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