A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834286



Internal ID15781556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777054..102778060hg38UCSC Ensembl
Innerchr14:103243391..103244397hg19UCSC Ensembl
Innerchr14:102313144..102314150hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381007
hg191007
hg181007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565959
Supporting Variants
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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