A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283702



Internal ID20492920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26078267..26078430hg38UCSC Ensembl
chr8:25935783..25935946hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283702
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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