A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665158



Internal ID21613463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36891723..36891723hg38UCSC Ensembl
chr22:37287765..37287765hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128696
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665158
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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