A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360479



Internal ID21018032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72588938..72590362hg38UCSC Ensembl
chr3:72638089..72639513hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381425
hg191425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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