A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4897n54



Internal ID18997073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6865482..7028228hg38UCSC Ensembl
chr16:6915483..7078229hg19UCSC Ensembl
chr16:6855484..7018230hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38162747
hg19162747
hg18162747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571376, nsv571379, nsv571380
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4897n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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