A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403095



Internal ID22460965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50755481..50756739hg38UCSC Ensembl
chr22:51193909..51195167hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403095
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