A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133208



Internal ID21498022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49922746..49922746hg38UCSC Ensembl
chr22:50316394..50316394hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670793
Supporting Variants
SamplesNA19238
Known GenesCRELD2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133208
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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