A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884109



Internal ID22659091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7661509..7662858hg38UCSC Ensembl
chr17:7564827..7566176hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884109
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