A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565982



Internal ID16353391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103124970..103132399hg38UCSC Ensembl
Innerchr14:103591307..103598736hg19UCSC Ensembl
Innerchr14:102661060..102668489hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg387430
hg197430
hg187430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3936n54
Supporting Variantsnssv834332, nssv834331
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565982
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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