A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390741



Internal ID21381876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76015327..76017868hg38UCSC Ensembl
chr13:76589463..76592004hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg382542
hg192542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705625
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390741
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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