A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768155



Internal ID20544015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13761139..13761139hg38UCSC Ensembl
chr4:13762763..13762763hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768155
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