A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053303



Internal ID18795834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70849608..70936254hg38UCSC Ensembl
Innerchr14:71316325..71402971hg19UCSC Ensembl
Innerchr14:70386078..70472724hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3886647
hg1986647
hg1886647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713524
Samples
Known GenesPCNX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053303
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