A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101378



Internal ID21505053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63169327..63169327hg38UCSC Ensembl
chr18:60836560..60836560hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652651
Supporting Variants
SamplesNA19650
Known GenesBCL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101378
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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