A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154384



Internal ID22084889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114855383..114908054hg38UCSC Ensembl
Outerchr8:114853580..114909926hg38UCSC Ensembl
Innerchr8:115867612..115920283hg19UCSC Ensembl
Outerchr8:115865809..115922155hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3856347
hg1956347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005020
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154384
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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