A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565973



Internal ID16353382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103124435..103133601hg38UCSC Ensembl
Innerchr14:103590772..103599938hg19UCSC Ensembl
Innerchr14:102660525..102669691hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg389167
hg199167
hg189167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3935n54
Supporting Variantsnssv834320
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565973
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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