A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514548



Internal ID22572506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86415058..86417724hg38UCSC Ensembl
chr9:89029973..89032639hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382667
hg192667
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514548
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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