A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982226



Internal ID21891569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:188017942..188023258hg38UCSC Ensembl
chr1:187987073..187992389hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg385317
hg195317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982226
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