A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3953n54



Internal ID20137377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104660017..104846598hg38UCSC Ensembl
chr14:105126354..105312935hg19UCSC Ensembl
chr14:104197399..104383980hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38186582
hg19186582
hg18186582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566053, nsv566059, nsv566060, nsv566052, nsv566063
Samples
Known GenesADSSL1, AKT1, INF2, LINC00638, MIR4710, SIVA1, ZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3953n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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