A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3987n54



Internal ID18996163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105461599..105499970hg38UCSC Ensembl
chr14:105927936..105966307hg19UCSC Ensembl
chr14:104998981..105037352hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3838372
hg1938372
hg1838372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566208, nsv566211
Samples
Known GenesC14orf80, CRIP1, CRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3987n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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