A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936862



Internal ID22712222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104767484..104800440hg38UCSC Ensembl
chr13:105419835..105452791hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3832957
hg1932957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936862
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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