A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426274



Internal ID21083827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140594746..140600869hg38UCSC Ensembl
chr8:141604845..141610968hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg386124
hg196124
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224615
Samples
Known GenesAGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426274
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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