A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111634



Internal ID22020867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63198864..63198864hg38UCSC Ensembl
chr18:60866097..60866097hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623755
Samples
Known GenesBCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111634
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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