A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670921



Internal ID21619226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48322398..48322398hg38UCSC Ensembl
chr22:48718210..48718210hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137220
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670921
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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