A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121771



Internal ID21419794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50212683..50212683hg38UCSC Ensembl
chr22:50651112..50651112hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668351
Supporting Variants
SamplesHG00731
Known GenesSELO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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