A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420418



Internal ID21077971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34922512..34939090hg38UCSC Ensembl
chr8:34780030..34796608hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3816579
hg1916579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420418
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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