A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566007



Internal ID16353416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521776..103523069hg38UCSC Ensembl
Innerchr14:103988113..103989406hg19UCSC Ensembl
Innerchr14:103057866..103059159hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381294
hg191294
hg181294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3943n54
Supporting Variantsnssv834373
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566007
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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