A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586664



Internal ID21535219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60087440..60087580hg38UCSC Ensembl
chr20:58662495..58662635hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117518
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586664
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer