A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5331n54



Internal ID20138755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89852186..89852755hg38UCSC Ensembl
chr16:89918594..89919163hg19UCSC Ensembl
chr16:88446095..88446664hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38570
hg19570
hg18570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573792, nsv573793, nsv573800, nsv573805
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5331n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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