A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658210



Internal ID21606515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112539838..112539838hg38UCSC Ensembl
chr13:113194152..113194152hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083946
SamplesHG00513
Known GenesTUBGCP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658210
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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