A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866924



Internal ID22641859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68692023..68694633hg38UCSC Ensembl
chr10:70451780..70454390hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382611
hg192611
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv189n209
Supporting Variantsnssv17463052
Samples
Known GenesTET1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866924
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