A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586233



Internal ID21534784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43995318..43995746hg38UCSC Ensembl
chr13:44569454..44569882hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082501
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586233
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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