A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275899



Internal ID20485117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6429032..6429032hg38UCSC Ensembl
chr19:6429043..6429043hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750374
Supporting Variants
Samples
Known GenesSLC25A41
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275899
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