A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564319



Internal ID16005042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35402011..35403586hg38UCSC Ensembl
Innerchr14:35871217..35872792hg19UCSC Ensembl
Innerchr14:34940968..34942543hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381576
hg191576
hg181576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825723
Samples
Known GenesNFKBIA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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