A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260902



Internal ID20470120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25527941..25528442hg38UCSC Ensembl
chr15:25773088..25773589hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260902
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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