A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5816n54



Internal ID22773711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:1899562..1980667hg38UCSC Ensembl
chr18:1899563..1980668hg19UCSC Ensembl
chr18:1889563..1970668hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3881106
hg1981106
hg1881106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576280, nsv576281
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5816n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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