A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5788n100



Internal ID20157404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115694413..115795583hg38UCSC Ensembl
chr5:115030110..115131280hg19UCSC Ensembl
chr5:115058009..115159179hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38101171
hg19101171
hg18101171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024641, nsv1021139
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)dgv5788n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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