A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566059



Internal ID16006782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104682318..104801891hg38UCSC Ensembl
Innerchr14:105148655..105268228hg19UCSC Ensembl
Innerchr14:104219700..104339273hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38119574
hg19119574
hg18119574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3953n54
Supporting Variantsnssv834441
Samples
Known GenesADSSL1, AKT1, INF2, SIVA1, ZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566059
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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