A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531130



Internal ID18482725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72854572..73897173hg38UCSC Ensembl
Innerchr14:73321280..74363876hg19UCSC Ensembl
Innerchr14:72391033..73433629hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381042602
hg191042597
hg181042597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035460
Supporting Variants
Samples
Known GenesACOT1, ACOT2, ACOT4, ACOT6, C14orf169, DCAF4, DNAL1, DPF3, ELMSAN1, HEATR4, MIR4505, NUMB, PAPLN, PNMA1, PSEN1, PTGR2, RBM25, ZFYVE1, ZNF410
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531130
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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