A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919268



Internal ID22694490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65676306..65676444hg38UCSC Ensembl
chr11:65443777..65443915hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919268
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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