A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883591



Internal ID22658573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36976654..36979706hg38UCSC Ensembl
chr20:35605057..35608109hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383053
hg193053
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883591
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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