A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360389



Internal ID21017942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166062301..166228700hg38UCSC Ensembl
chr3:165780089..165946488hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38166400
hg19166400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5076n223
Supporting Variantsnssv18208545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360389
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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