A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858066



Internal ID22633001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90263445..90309588hg38UCSC Ensembl
chr10:92023202..92069345hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3846144
hg1946144
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858066
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