A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959320



Internal ID22734352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17900617..17902558hg38UCSC Ensembl
chr21:19272934..19274875hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381942
hg191942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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