A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493285



Internal ID21150838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49859999..49876936hg38UCSC Ensembl
chr13:50434135..50451072hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3816938
hg1916938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493285
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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