A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908413



Internal ID22683623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102264663..102265433hg38UCSC Ensembl
chr11:102135394..102136164hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908413
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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