A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283819



Internal ID20493037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90685034..90685854hg38UCSC Ensembl
chr8:91697262..91698082hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283819
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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