A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952085



Internal ID22727414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11628936..11629300hg38UCSC Ensembl
chrUn_gl000229:17561..17925hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952085
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