A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851333



Internal ID22626268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78090564..78098059hg38UCSC Ensembl
chr10:79850321..79857816hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387496
hg197496
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851333
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