A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479943



Internal ID21137496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94774225..94793278hg38UCSC Ensembl
chr13:95426479..95445532hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3819054
hg1919054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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