A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056518



Internal ID21965751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41744480..41744804hg38UCSC Ensembl
chr22:42140484..42140808hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640478
Samples
Known GenesMEI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056518
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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