A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv40n97



Internal ID22815437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89178916..89194672hg38UCSC Ensembl
chr10:90938673..90954429hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3815757
hg1915757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154645, nsv1154644
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv40n97
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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