A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3592n54



Internal ID22771487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27039536..27127724hg38UCSC Ensembl
chr14:27508742..27596930hg19UCSC Ensembl
chr14:26578582..26666770hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3888189
hg1988189
hg1888189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564118, nsv564117
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3592n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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