A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896414



Internal ID22671507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28882592..28906719hg38UCSC Ensembl
chr4:28884214..28908341hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3824128
hg1924128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896414
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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