A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600012



Internal ID21548650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133291288..133292478hg38UCSC Ensembl
chr10:135104792..135105982hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069140
SamplesHG00731
Known GenesTUBGCP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600012
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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