A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600058



Internal ID21792105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38477240..38477240hg38UCSC Ensembl
chr15:38769441..38769441hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082187
Supporting Variants
Samples
Known GenesFAM98B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600058
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer