A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3935n54



Internal ID22771830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103124435..103135315hg38UCSC Ensembl
chr14:103590772..103601652hg19UCSC Ensembl
chr14:102660525..102671405hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3810881
hg1910881
hg1810881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565977, nsv565974, nsv565973, nsv565975
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3935n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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