A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146891



Internal ID346097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11780629..11977000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38196372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146891
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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