A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029580



Internal ID21938923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88858008..89336256hg38UCSC Ensembl
chr13:89510262..89988510hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38478249
hg19478249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029580
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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