A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4853n54



Internal ID20138277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1372825..1376726hg38UCSC Ensembl
chr16:1422826..1426727hg19UCSC Ensembl
chr16:1362827..1366728hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383902
hg193902
hg183902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571153, nsv571159, nsv571154, nsv571152
Samples
Known GenesUNKL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4853n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer