A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286860



Internal ID20496078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98041800..98041800hg38UCSC Ensembl
chr15:98585029..98585029hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766584
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286860
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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