A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587214



Internal ID21535774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63212067..63212615hg38UCSC Ensembl
chr18:60879300..60879848hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101380
SamplesHG01505
Known GenesBCL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587214
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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