A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544401



Internal ID18398791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144492929..144495435hg38UCSC Ensembl
Outerchr8:144492578..144495855hg38UCSC Ensembl
Innerchr8:145718312..145720818hg19UCSC Ensembl
Outerchr8:145717961..145721238hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383278
hg193278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743148
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544401
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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