A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291828



Internal ID20501046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92777534..92780384hg38UCSC Ensembl
chr8:93789762..93792612hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382851
hg192851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743036
Supporting Variants
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291828
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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