A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5939n54



Internal ID22773834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53603119..53612586hg38UCSC Ensembl
chr18:51129489..51138956hg19UCSC Ensembl
chr18:49383487..49392954hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg389468
hg199468
hg189468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576941, nsv576942, nsv576943
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5939n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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