A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656644



Internal ID21604949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44756583..44756583hg38UCSC Ensembl
chr19:45259840..45259840hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105288
SamplesHG02818
Known GenesBCL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656644
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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