A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432483



Internal ID21090036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116617221..116632864hg38UCSC Ensembl
chr8:117629460..117645103hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3815644
hg1915644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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