A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9482n54



Internal ID22777377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:467509..472407hg38UCSC Ensembl
chr5:467624..472522hg19UCSC Ensembl
chr5:520624..525522hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg384899
hg194899
hg184899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596636, nsv596670
Samples
Known GenesPP7080
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9482n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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