A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043395



Internal ID21952699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47938704..47965996hg38UCSC Ensembl
chr22:48334453..48361745hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3827293
hg1927293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043395
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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