A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852890



Internal ID22627825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87561873..87584245hg38UCSC Ensembl
chr10:89321630..89344002hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3822373
hg1922373
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852890
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