A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514552



Internal ID22572510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86583824..86586453hg38UCSC Ensembl
chr9:89198739..89201368hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382630
hg192630
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514552
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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