A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526368



Internal ID302499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2254953..2775167hg38UCSC Ensembl
chr18:2254953..2775165hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38520215
hg19520213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715860
Samples
Known GenesCBX3P2, METTL4, NDC80, SMCHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526368
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