A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834325



Internal ID16128281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103124970..103130272hg38UCSC Ensembl
Innerchr14:103591307..103596609hg19UCSC Ensembl
Innerchr14:102661060..102666362hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg385303
hg195303
hg185303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565978
Supporting Variants
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834325
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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