A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045288



Internal ID18787819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35266680..35318983hg38UCSC Ensembl
Innerchr14:35735886..35788189hg19UCSC Ensembl
Innerchr14:34805637..34857940hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3852304
hg1952304
hg1852304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1869n100
Supporting Variantsnssv3528619
Samples
Known GenesKIAA0391, PSMA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045288
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