A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154377



Internal ID22084882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:104872361..104895233hg38UCSC Ensembl
Outerchr8:104872256..104897519hg38UCSC Ensembl
Innerchr8:105884589..105907461hg19UCSC Ensembl
Outerchr8:105884484..105909747hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3825264
hg1925264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004978
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154377
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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