A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486166



Internal ID21143719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57490724..57515408hg38UCSC Ensembl
chr13:58064858..58089542hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3824685
hg1924685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486166
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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