A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360862



Internal ID21018415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82990592..83156655hg38UCSC Ensembl
chr3:83039743..83205806hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38166064
hg19166064
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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