A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859550



Internal ID22634485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45418169..45420868hg38UCSC Ensembl
chr10:45913617..45916316hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464584, nssv17452242
Samples
Known GenesALOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859550
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