A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4876n54



Internal ID18997052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3655014..3668847hg38UCSC Ensembl
chr16:3705015..3718848hg19UCSC Ensembl
chr16:3645016..3658849hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3813834
hg1913834
hg1813834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571258, nsv571257
SamplesHGDP01066
Known GenesDNASE1, TRAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4876n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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