A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853152



Internal ID22628087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78562026..78567313hg38UCSC Ensembl
chr9:81176942..81182229hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385288
hg195288
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853152
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