A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514565



Internal ID22572523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87057996..87059195hg38UCSC Ensembl
chr9:89672911..89674110hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514565
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