A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3936n54



Internal ID22771831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103124673..103132399hg38UCSC Ensembl
chr14:103591010..103598736hg19UCSC Ensembl
chr14:102660763..102668489hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg387727
hg197727
hg187727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565984, nsv565982, nsv565985, nsv565976
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3936n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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