A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279142



Internal ID20488360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122563428..122563428hg38UCSC Ensembl
chr8:123575667..123575667hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385906
hg195906
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279142
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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