A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418314



Internal ID21075867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20332364..20333122hg38UCSC Ensembl
chr8:20189875..20190633hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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