A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982444



Internal ID21891787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210283157..210285248hg38UCSC Ensembl
chr1:210456502..210458593hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg382092
hg192092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982444
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