A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566002



Internal ID16353411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521722..103523176hg38UCSC Ensembl
Innerchr14:103988059..103989513hg19UCSC Ensembl
Innerchr14:103057812..103059266hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381455
hg191455
hg181455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3943n54
Supporting Variantsnssv834362, nssv834361
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566002
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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