A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105287



Internal ID21458426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44751439..44751439hg38UCSC Ensembl
chr19:45254696..45254696hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382994
hg192994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659538
Supporting Variants
SamplesHG02587
Known GenesBCL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105287
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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