A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067435



Internal ID18809966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:475761..677639hg38UCSC Ensembl
Innerchr18:475761..677639hg19UCSC Ensembl
Innerchr18:465761..667639hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38201879
hg19201879
hg18201879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3307n100
Supporting Variantsnssv3563893
Samples
Known GenesC18orf56, CETN1, CLUL1, COLEC12, ENOSF1, TYMS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067435
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