A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154620



Internal ID22085125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:67567814..67586984hg38UCSC Ensembl
Outerchr10:67564372..67590805hg38UCSC Ensembl
Innerchr10:69327572..69346742hg19UCSC Ensembl
Outerchr10:69324130..69350563hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3826434
hg1926434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005883
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154620
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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