A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058739



Internal ID21967972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47178092..47179595hg38UCSC Ensembl
chr22:47573845..47575348hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381504
hg191504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058739
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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