A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886021



Internal ID22661008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23150049..23158048hg38UCSC Ensembl
chr20:23130686..23138685hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886021
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