A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127600



Internal ID21489177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28195922..28213764hg38UCSC Ensembl
chr22:28591910..28609752hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3817843
hg1917843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597329
Supporting Variants
SamplesNA18939
Known GenesTTC28
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127600
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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