A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6118n54



Internal ID20139542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79748181..79788559hg38UCSC Ensembl
chr18:77508181..77548559hg19UCSC Ensembl
chr18:75609169..75649547hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3840379
hg1940379
hg1840379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577911, nsv577910
SamplesHGDP00954, HGDP00823
Known GenesCTDP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6118n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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