A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132037



Internal ID21424747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50166025..50166025hg38UCSC Ensembl
chr22:50604454..50604454hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664682
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132037
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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