A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4895n54



Internal ID20138319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6812010..6914962hg38UCSC Ensembl
chr16:6862011..6964963hg19UCSC Ensembl
chr16:6802012..6904964hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38102953
hg19102953
hg18102953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571368, nsv571369, nsv571374, nsv571372
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4895n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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