A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481036



Internal ID22538940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12111767..12113664hg38UCSC Ensembl
chr1:142632662..142634563hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg381898
hg191902
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882530
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481036
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