A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051901



Internal ID21961134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11454640..11455409hg38UCSC Ensembl
chrUn_gl000233:26584..27353hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051901
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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