A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834324



Internal ID16128280
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 StatusS
Merged Variantsnsv565977
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)nssv834324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer