A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618093



Internal ID21566398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189896183..189896183hg38UCSC Ensembl
chr2:190760909..190760909hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110941
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618093
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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