A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9635n54



Internal ID22777530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18838025..18976852hg38UCSC Ensembl
chr5:18838134..18976961hg19UCSC Ensembl
chr5:18873891..19012718hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38138828
hg19138828
hg18138828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597396, nsv597381, nsv597380
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9635n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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