A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052389



Internal ID19141608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65789063..65854844hg38UCSC Ensembl
Innerchr14:66255781..66321562hg19UCSC Ensembl
Innerchr14:65325534..65391315hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3865782
hg1965782
hg1865782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1926n100
Supporting Variantsnssv3531082
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)nsv1052389
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