A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929820



Internal ID22705079
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 Variantsnssv17377794
Samples
Known GenesBCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929820
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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