A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279576



Internal ID20488794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104492993..104493369hg38UCSC Ensembl
chr9:107255274..107255650hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279576
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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