A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043558



Internal ID21952852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47626328..47626383hg38UCSC Ensembl
chr22:48022077..48022132hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639011
Samples
Known GenesLINC00898
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043558
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