A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589643



Internal ID21538208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34132886..34133061hg38UCSC Ensembl
chr20:32720692..32720867hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116540
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589643
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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