A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264327



Internal ID20473545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29660520..29660520hg38UCSC Ensembl
chr8:29518036..29518036hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264327
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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