A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854630



Internal ID22629565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68867543..68873864hg38UCSC Ensembl
chr11:68635011..68641332hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg386322
hg196322
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464342, nssv17452350, nssv17468147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854630
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