A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667668



Internal ID21615973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35533643..35533643hg38UCSC Ensembl
chr22:35929690..35929690hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138879
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667668
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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