A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754619



Internal ID20530479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54325413..54325413hg38UCSC Ensembl
chr4:55191580..55191580hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754619
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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