A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590076



Internal ID21538644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109383166..109383265hg38UCSC Ensembl
chr13:110035513..110035612hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091781
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590076
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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