A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4899n54



Internal ID20138323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6987386..7019055hg38UCSC Ensembl
chr16:7037387..7069056hg19UCSC Ensembl
chr16:6977388..7009057hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3831670
hg1931670
hg1831670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571386, nsv571387
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4899n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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