A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566060



Internal ID16006783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104682318..104844912hg38UCSC Ensembl
Innerchr14:105148655..105311249hg19UCSC Ensembl
Innerchr14:104219700..104382294hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38162595
hg19162595
hg18162595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3953n54
Supporting Variantsnssv834442
Samples
Known GenesADSSL1, AKT1, INF2, LINC00638, SIVA1, ZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566060
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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