A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565977



Internal ID16353386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103124673..103135315hg38UCSC Ensembl
Innerchr14:103591010..103601652hg19UCSC Ensembl
Innerchr14:102660763..102671405hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3810643
hg1910643
hg1810643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3935n54
Supporting Variantsnssv834324
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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