A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882639



Internal ID22657616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42813152..42815101hg38UCSC Ensembl
chr21:44233262..44235211hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381950
hg191950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480900, nssv17488907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882639
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