A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613052



Internal ID20986123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106848352..106974652hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38126301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613052
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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