A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428867



Internal ID21086420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20300481..20308183hg38UCSC Ensembl
chr8:20157992..20165694hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg387703
hg197703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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