A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483493



Internal ID22541400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39705241..39706340hg38UCSC Ensembl
chr22:40101246..40102345hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483493
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer