A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890707



Internal ID19185009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109456588..109629795hg38UCSC Ensembl
Outerchr5:109456588..109629795hg38UCSC Ensembl
Innerchr5:108792289..108965496hg19UCSC Ensembl
Outerchr5:108792289..108965496hg19UCSC Ensembl
Innerchr5:108820188..108993395hg18UCSC Ensembl
Outerchr5:108820188..108993395hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38173208
hg19173208
hg18173208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790782
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890707
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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