A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565972



Internal ID16353381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103112298..103135941hg38UCSC Ensembl
Innerchr14:103578635..103602278hg19UCSC Ensembl
Innerchr14:102648388..102672031hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3823644
hg1923644
hg1823644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834319
Samples
Known GenesTNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565972
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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