A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866564



Internal ID22641499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11627628..11630177hg38UCSC Ensembl
chr8:11485137..11487686hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866564
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