A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282203



Internal ID20491421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87818962..87818962hg38UCSC Ensembl
chr9:90433877..90433877hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282203
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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