A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3774n54



Internal ID22771669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73556034..73580812hg38UCSC Ensembl
chr14:74022738..74047516hg19UCSC Ensembl
chr14:73092491..73117269hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3824779
hg1924779
hg1824779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565170, nsv565166, nsv565171, nsv565164, nsv565167, nsv565168, nsv565169, nsv565165, nsv565163
Samples
Known GenesACOT2, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3774n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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