A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483867



Internal ID21141420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46806901..46811300hg38UCSC Ensembl
chr13:47381036..47385435hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1821n223
Supporting Variantsnssv18182440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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