A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3594n54



Internal ID22771489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27650395..27734481hg38UCSC Ensembl
chr14:28119601..28203687hg19UCSC Ensembl
chr14:27189441..27273527hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3884087
hg1984087
hg1884087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564135, nsv564134
SamplesHGDP01034
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3594n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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