A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4828n54



Internal ID18997004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:760143..828324hg38UCSC Ensembl
chr16:810143..878324hg19UCSC Ensembl
chr16:750144..818325hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3868182
hg1968182
hg1868182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571027, nsv571041
Samples
Known GenesCHTF18, GNG13, MIR662, MSLN, PRR25, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4828n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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