A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5885n54



Internal ID20139309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37461933..37487164hg38UCSC Ensembl
chr18:35041896..35067127hg19UCSC Ensembl
chr18:33295894..33321125hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3825232
hg1925232
hg1825232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576659, nsv576658
Samples1780854492_A
Known GenesCELF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5885n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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