A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668251



Internal ID21616556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23334204..23334204hg38UCSC Ensembl
chr20:23314841..23314841hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115894
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668251
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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