A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154387



Internal ID22084892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119278057..119284309hg38UCSC Ensembl
Outerchr8:119275864..119298868hg38UCSC Ensembl
Innerchr8:120290297..120296549hg19UCSC Ensembl
Outerchr8:120288104..120311108hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3823005
hg1923005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005042, nssv4005041, nssv4005044, nssv4005043
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154387
Frequency
Sample Size131
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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