A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564409



Internal ID16351818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38401252..38460850hg38UCSC Ensembl
Innerchr14:38870456..38930054hg19UCSC Ensembl
Innerchr14:37940207..37999805hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3859599
hg1959599
hg1859599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv826026
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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