A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262899



Internal ID20472117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90146179..90146179hg38UCSC Ensembl
chr9:92908461..92908461hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262899
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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