A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv101n97



Internal ID22815498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93184918..93227315hg38UCSC Ensembl
chr15:93728147..93770544hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3842398
hg1942398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155209, nsv1155207, nsv1155208
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv101n97
Frequency
Sample Size131
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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