A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729127



Internal ID152793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41189207..41211700hg38UCSC Ensembl
chr22:41585211..41607704hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3822494
hg1922494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545120
Supporting Variants
Samples
Known GenesL3MBTL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729127
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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