A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566701



Internal ID18767777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138472082..138480811hg38UCSC Ensembl
Outerchr5:138470812..138481811hg38UCSC Ensembl
Innerchr5:137807771..137816500hg19UCSC Ensembl
Outerchr5:137806501..137817500hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3811000
hg1911000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765448
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566701
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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