A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135841



Internal ID21462364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38666192..38666261hg38UCSC Ensembl
chr22:39062197..39062266hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590046
Supporting Variants
SamplesHG02818
Known GenesCBY1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135841
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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