A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584627



Internal ID21533169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33277019..33277187hg38UCSC Ensembl
chr20:31864825..31864993hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116172
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584627
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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