A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154361



Internal ID22084866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55076243..55091792hg38UCSC Ensembl
Outerchr8:55074281..55095175hg38UCSC Ensembl
Innerchr8:55988803..56004352hg19UCSC Ensembl
Outerchr8:55986841..56007735hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3820895
hg1920895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004917
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154361
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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