A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1935n100



Internal ID20153551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73522514..73583548hg38UCSC Ensembl
chr14:73989218..74050252hg19UCSC Ensembl
chr14:73058971..73120005hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3861035
hg1961035
hg1861035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052576, nsv1053648, nsv1038801
Samples
Known GenesACOT1, ACOT2, HEATR4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1935n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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