A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039859



Internal ID18782390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105563288..105795460hg38UCSC Ensembl
Innerchr14:106029625..106261807hg19UCSC Ensembl
Innerchr14:105100670..105332852hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38232173
hg19232183
hg18232183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1984n100
Supporting Variantsnssv3529829
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039859
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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