A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129728



Internal ID21474527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19240263..19240263hg38UCSC Ensembl
chr22:19227786..19227786hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669884
Supporting Variants
SamplesHG03371
Known GenesCLTCL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129728
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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