A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987807



Internal ID21897150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223480008..223490018hg38UCSC Ensembl
chr2:224344726..224354736hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3810011
hg1910011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987807
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