A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586752



Internal ID21535308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40969382..40969483hg38UCSC Ensembl
chr20:39598022..39598123hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116411
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586752
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