A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3937n54



Internal ID22771832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103124970..103131228hg38UCSC Ensembl
chr14:103591307..103597565hg19UCSC Ensembl
chr14:102661060..102667318hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg386259
hg196259
hg186259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565980, nsv565979, nsv565978, nsv565983, nsv565981
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3937n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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