A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988158



Internal ID21897501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222156662..222156767hg38UCSC Ensembl
chr2:223021381..223021486hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988158
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