A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3769n54



Internal ID20137193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73533942..73538343hg38UCSC Ensembl
chr14:74000646..74005047hg19UCSC Ensembl
chr14:73070399..73074800hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384402
hg194402
hg184402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565146, nsv565140, nsv565136
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3769n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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