A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945926



Internal ID22721409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108592054..108592334hg38UCSC Ensembl
chr13:109244402..109244682hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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