A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880208



Internal ID22655178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29455067..29457287hg38UCSC Ensembl
chr17:27782085..27784305hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473051
Samples
Known GenesTAOK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880208
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