A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565976



Internal ID16353385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103124673..103132335hg38UCSC Ensembl
Innerchr14:103591010..103598672hg19UCSC Ensembl
Innerchr14:102660763..102668425hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg387663
hg197663
hg187663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3936n54
Supporting Variantsnssv834323
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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