A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044069



Internal ID19133288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104322764..104471971hg38UCSC Ensembl
Innerchr14:104789101..104938308hg19UCSC Ensembl
Innerchr14:103860146..104009353hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38149208
hg19149208
hg18149208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1979n100
Supporting Variantsnssv3533564
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)nsv1044069
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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