A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5323n54



Internal ID18997499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89647647..89648410hg38UCSC Ensembl
chr16:89714055..89714818hg19UCSC Ensembl
chr16:88241556..88242319hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38764
hg19764
hg18764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573740, nsv573741, nsv573742
Samples
Known GenesCHMP1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5323n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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