A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566646



Internal ID18767722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131154080..131154377hg38UCSC Ensembl
Outerchr5:131154049..131154414hg38UCSC Ensembl
Innerchr5:130489773..130490070hg19UCSC Ensembl
Outerchr5:130489742..130490107hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765393
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566646
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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