A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429458



Internal ID21087011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114297801..114348700hg38UCSC Ensembl
chr8:115310030..115360929hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3850900
hg1950900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7468n223
Supporting Variantsnssv18220965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429458
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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