A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601841



Internal ID21550492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48730192..48730335hg38UCSC Ensembl
chr18:46256563..46256706hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101155
SamplesHG03065
Known GenesCTIF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601841
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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