A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741898



Internal ID18716144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17104721..17105016hg38UCSC Ensembl
Outerchr8:17104663..17105071hg38UCSC Ensembl
Innerchr8:16962230..16962525hg19UCSC Ensembl
Outerchr8:16962172..16962580hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543151
Supporting Variants
Samples
Known GenesMICU3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741898
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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