A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951376



Internal ID22726741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33284554..33284916hg38UCSC Ensembl
chr22:33680540..33680902hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400029
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951376
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