A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375346



Internal ID21032899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83414742..83424112hg38UCSC Ensembl
chr3:83463893..83473263hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg389371
hg199371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375346
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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