A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139167



Internal ID21418583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31591944..31592266hg38UCSC Ensembl
chr22:31987930..31988252hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601313
Supporting Variants
SamplesHG00731
Known GenesSFI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139167
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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