A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851210



Internal ID22626145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125816026..125826241hg38UCSC Ensembl
chr11:125685921..125696136hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3810216
hg1910216
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851210
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