A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416409



Internal ID21073962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89347507..89366520hg38UCSC Ensembl
chr8:90359736..90378749hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3819014
hg1919014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416409
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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