A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422516



Internal ID21080069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109199656..109224385hg38UCSC Ensembl
chr8:110211885..110236614hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3824730
hg1924730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422516
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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