A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582877



Internal ID21531394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126640079..126640405hg38UCSC Ensembl
chr3:126358922..126359248hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122474
SamplesHG00731
Known GenesTXNRD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582877
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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