A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566822



Internal ID18767898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152381371..152381658hg38UCSC Ensembl
Outerchr5:152381323..152381709hg38UCSC Ensembl
Innerchr5:151760932..151761219hg19UCSC Ensembl
Outerchr5:151760884..151761270hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765569
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566822
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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