A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3767n54



Internal ID20137191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73532551..73545443hg38UCSC Ensembl
chr14:73999255..74012147hg19UCSC Ensembl
chr14:73069008..73081900hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3812893
hg1912893
hg1812893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565131, nsv565142, nsv565141, nsv565138
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3767n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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