A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645166



Internal ID21593471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109228040..109228040hg38UCSC Ensembl
chr11:109098767..109098767hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072668
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645166
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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