A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5325n54



Internal ID20138749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89830015..89830866hg38UCSC Ensembl
chr16:89896423..89897274hg19UCSC Ensembl
chr16:88423924..88424775hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38852
hg19852
hg18852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573752, nsv573760, nsv573750, nsv573751
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5325n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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