A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565698



Internal ID18766774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25822082..25826581hg38UCSC Ensembl
Outerchr5:25821454..25826748hg38UCSC Ensembl
Innerchr5:25822191..25826690hg19UCSC Ensembl
Outerchr5:25821563..25826857hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg385295
hg195295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764445
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565698
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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