A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859298



Internal ID22634233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18295069..18317067hg38UCSC Ensembl
chrUn_gl000212:123821..145819hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3821999
hg1921999
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458420, nssv17458094, nssv17466077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859298
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