A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146423



Internal ID345628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12169900..12179555hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146423
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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