A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458053



Internal ID22515934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103596142..103601429hg38UCSC Ensembl
chr14:104062479..104067766hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg385288
hg195288
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860248
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458053
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