A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670169



Internal ID21618476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37461526..37461526hg38UCSC Ensembl
chr22:37857564..37857564hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126387
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670169
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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