A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955402



Internal ID22730604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27793331..27793384hg38UCSC Ensembl
chr22:28189319..28189372hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397076
Samples
Known GenesMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955402
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