A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429368



Internal ID21086921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89898001..89907800hg38UCSC Ensembl
chr8:90910229..90920028hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7417n223
Supporting Variantsnssv18228581
Samples
Known GenesOSGIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429368
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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