A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866805



Internal ID22641740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133261436..133265727hg38UCSC Ensembl
chr9:136136839..136141138hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg384292
hg194300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511674
Samples
Known GenesABO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866805
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