A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566006



Internal ID16353415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521776..103522835hg38UCSC Ensembl
Innerchr14:103988113..103989172hg19UCSC Ensembl
Innerchr14:103057866..103058925hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381060
hg191060
hg181060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3942n54
Supporting Variantsnssv834372
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566006
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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