A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5826n54



Internal ID22773721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5294903..5296461hg38UCSC Ensembl
chr18:5294902..5296460hg19UCSC Ensembl
chr18:5284902..5286460hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381559
hg191559
hg181559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576340, nsv576346, nsv576347, nsv576342
Samples
Known GenesZBTB14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5826n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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