A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9532n54



Internal ID22777427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1178396..1180452hg38UCSC Ensembl
chr5:1178511..1180567hg19UCSC Ensembl
chr5:1231511..1233567hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382057
hg192057
hg182057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596847, nsv596837, nsv596849, nsv596846
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9532n54
Frequency
Sample Size17421
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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