A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958603



Internal ID22733665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41081568..41087592hg38UCSC Ensembl
chr21:42453495..42459519hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg386025
hg196025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958603
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