A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261719



Internal ID20470937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86750084..86750169hg38UCSC Ensembl
chr9:89364999..89365084hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261719
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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