A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3744n54



Internal ID20137168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69572870..69574240hg38UCSC Ensembl
chr14:70039587..70040957hg19UCSC Ensembl
chr14:69109340..69110710hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381371
hg191371
hg181371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565006, nsv565005
Samples
Known GenesCCDC177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3744n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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