A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259037



Internal ID20468225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68229751..68229751hg38UCSC Ensembl
chr15:68522089..68522089hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259037
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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