A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653369



Internal ID21601674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128868352..128868352hg38UCSC Ensembl
chr11:128738247..128738247hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072801
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653369
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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