A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565985



Internal ID16353394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103125002..103132399hg38UCSC Ensembl
Innerchr14:103591339..103598736hg19UCSC Ensembl
Innerchr14:102661092..102668489hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg387398
hg197398
hg187398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3936n54
Supporting Variantsnssv834335
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565985
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