A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997446



Internal ID21906789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4412698..4414133hg38UCSC Ensembl
chr4:4414425..4415860hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550359
Samples
Known GenesNSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997446
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