A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452895



Internal ID231037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13255468..13289803hg38UCSC Ensembl
chr4:13257092..13291427hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3834336
hg1934336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv368n206
Supporting Variantsnssv16948176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452895
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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