A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359288



Internal ID21016841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170060854..170117962hg38UCSC Ensembl
chr3:169778642..169835750hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3857109
hg1957109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209203
Samples
Known GenesGPR160, PHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359288
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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