A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650587



Internal ID21598892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26727077..26727077hg38UCSC Ensembl
chr18:24307041..24307041hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100823
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650587
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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