A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056821



Internal ID21966056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40033142..40036071hg38UCSC Ensembl
chr22:40429146..40432075hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382930
hg192930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640976
Samples
Known GenesLOC100130899
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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