A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861984



Internal ID22636919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18196940..18200965hg38UCSC Ensembl
chrUn_gl000212:25692..29717hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384026
hg194026
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv504n209
Supporting Variantsnssv17464412, nssv17460466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861984
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