A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3772n54



Internal ID20137196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73539224..73548935hg38UCSC Ensembl
chr14:74005928..74015639hg19UCSC Ensembl
chr14:73075681..73085392hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389712
hg199712
hg189712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565155, nsv565152
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3772n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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