A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563607



Internal ID16351016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18563916..18602856hg38UCSC Ensembl
Innerchr14:19340393..19379333hg19UCSC Ensembl
Innerchr14:18410393..18449333hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg3838941
hg1938941
hg1838941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv821322
Samples
Known GenesOR11H12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563607
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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