A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588878



Internal ID21537442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3441163..3441400hg38UCSC Ensembl
chr20:3421810..3422047hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116552
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588878
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