A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661763



Internal ID21610068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59436132..59436132hg38UCSC Ensembl
chr18:57103364..57103364hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101353
SamplesNA20509
Known GenesCCBE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661763
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