A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418381



Internal ID21075934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116410621..116412264hg38UCSC Ensembl
chr8:117422859..117424502hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381644
hg191644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418381
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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