A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593741



Internal ID21542332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36418351..36418476hg38UCSC Ensembl
chr13:36992488..36992613hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097471
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593741
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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