A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154398



Internal ID22084903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139100475..139103770hg38UCSC Ensembl
Outerchr8:139098174..139105176hg38UCSC Ensembl
Innerchr8:140112718..140116013hg19UCSC Ensembl
Outerchr8:140110417..140117419hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg387003
hg197003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005062
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154398
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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