A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430406



Internal ID21087959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141184017..141201438hg38UCSC Ensembl
chr8:142194116..142211537hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3817422
hg1917422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230604
Samples
Known GenesDENND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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