A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279568



Internal ID20488786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82040965..82040965hg38UCSC Ensembl
chr8:82953200..82953200hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279568
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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