A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594761



Internal ID21543361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27051818..27051885hg38UCSC Ensembl
chr13:27625955..27626022hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086066
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594761
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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