A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486559



Internal ID21144112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57842096..57890993hg38UCSC Ensembl
chr13:58416230..58465127hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3848898
hg1948898
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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