A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890755



Internal ID19185057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153169261..153282556hg38UCSC Ensembl
Outerchr5:153169261..153282556hg38UCSC Ensembl
Innerchr5:152548821..152662116hg19UCSC Ensembl
Outerchr5:152548821..152662116hg19UCSC Ensembl
Innerchr5:152529014..152642309hg18UCSC Ensembl
Outerchr5:152529014..152642309hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38113296
hg19113296
hg18113296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788985
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890755
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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