A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045990



Internal ID18788521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106625325..106877229hg38UCSC Ensembl
Innerchr14:107081339..107285437hg19UCSC Ensembl
Innerchr14:106152384..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38251905
hg19204099
hg18204099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2152n100
Supporting Variantsnssv3533059
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045990
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