A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5589n100



Internal ID22791676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17601432..17794454hg38UCSC Ensembl
chr5:17601541..17794563hg19UCSC Ensembl
chr5:17644644..17830320hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38193023
hg19193023
hg18185677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021109, nsv1027181
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5589n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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