A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834248



Internal ID15781518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102776388..102778185hg38UCSC Ensembl
Innerchr14:103242725..103244522hg19UCSC Ensembl
Innerchr14:102312478..102314275hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381798
hg191798
hg181798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565952
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)nssv834248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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