A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3771n54



Internal ID20137195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73539224..73545443hg38UCSC Ensembl
chr14:74005928..74012147hg19UCSC Ensembl
chr14:73075681..73081900hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg386220
hg196220
hg186220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565149, nsv565151, nsv565150
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3771n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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