A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666815



Internal ID21615123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28537293..28537293hg38UCSC Ensembl
chr22:28933281..28933281hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131445, nssv17131529
SamplesHG01505, HG00512
Known GenesTTC28
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666815
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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