A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590880



Internal ID21539450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46466193..46466287hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070064
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590880
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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