A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563608



Internal ID16351017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18566430..18608995hg38UCSC Ensembl
Innerchr14:19342907..19385472hg19UCSC Ensembl
Innerchr14:18412907..18455472hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg3842566
hg1942566
hg1842566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv821323
Samples
Known GenesOR11H12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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