A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997442



Internal ID21906785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37585181..37585606hg38UCSC Ensembl
chr4:37586803..37587228hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551458
Samples
Known GenesC4orf19
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997442
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer