A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651831



Internal ID21600136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108258201..108258201hg38UCSC Ensembl
chr13:108910549..108910549hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098058
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651831
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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