A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042874



Internal ID21952186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6448845..6448924hg38UCSC Ensembl
chr19:6448856..6448935hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624036
Samples
Known GenesSLC25A23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042874
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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