A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866422



Internal ID22641357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115417383..115418882hg38UCSC Ensembl
chr8:116429611..116431110hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505584
Samples
Known GenesTRPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866422
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