A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122403



Internal ID21485777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31591590..31591768hg38UCSC Ensembl
chr22:31987576..31987754hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584825
Supporting Variants
SamplesNA12878
Known GenesSFI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122403
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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