A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051586



Internal ID21960819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45423945..45424103hg38UCSC Ensembl
chr22:45819825..45819983hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641183
Samples
Known GenesRIBC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051586
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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