A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566189



Internal ID18767265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:82908752..82908871hg38UCSC Ensembl
Outerchr5:82908750..82908874hg38UCSC Ensembl
Innerchr5:82204571..82204690hg19UCSC Ensembl
Outerchr5:82204569..82204693hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764936
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566189
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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