A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127104



Internal ID21483821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20338388..20338388hg38UCSC Ensembl
chr22:20325911..20325911hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg387728
hg197728
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669515
Supporting Variants
SamplesNA12329
Known GenesLOC729444
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127104
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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