A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4891n54



Internal ID18997067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6598151..6639091hg38UCSC Ensembl
chr16:6648152..6689092hg19UCSC Ensembl
chr16:6588153..6629093hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3840941
hg1940941
hg1840941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571338, nsv571339
SamplesHGDP00658
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4891n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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