A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652956



Internal ID21601261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104495545..104495545hg38UCSC Ensembl
chr13:105147895..105147895hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097286
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652956
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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