A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146258



Internal ID345463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23841564..23957564hg38UCSC Ensembl
chr22:24183751..24299751hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38116001
hg19116001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728021
Samples
Known GenesGSTT2, GSTT2B, LOC284889, MIF, SLC2A11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146258
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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