A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483924



Internal ID21141477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110942300..110991590hg38UCSC Ensembl
chr13:111594647..111643937hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3849291
hg1949291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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