A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010548



Internal ID21919891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23549706..23550346hg38UCSC Ensembl
chr8:23407219..23407859hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563833
Samples
Known GenesSLC25A37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010548
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