A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146888



Internal ID346094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18156010..18190010hg38UCSC Ensembl
chr22:18638777..18672777hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3834001
hg1934001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727563
Samples
Known GenesUSP18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146888
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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