A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17512116



Internal ID22570068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18153344..18156180hg38UCSC Ensembl
chr9:18153342..18156178hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg382837
hg192837
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17512116
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