A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664779



Internal ID21613086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21573399..21573399hg38UCSC Ensembl
chr20:21554037..21554037hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116468
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664779
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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