A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136746



Internal ID21439252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50337600..50337662hg38UCSC Ensembl
chr22:50776029..50776091hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592592
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136746
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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