A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586762



Internal ID21535318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12507818..12507898hg38UCSC Ensembl
chr20:12488466..12488546hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115814
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586762
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