A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995601



Internal ID21904944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122623231..122626259hg38UCSC Ensembl
chr4:123544386..123547414hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg383029
hg193029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554774
Samples
Known GenesIL21-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995601
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