A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054012



Internal ID21963245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49784169..49784251hg38UCSC Ensembl
chr22:50177817..50177899hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647844
Samples
Known GenesBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054012
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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