A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235112



Internal ID20802152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141149018..141157867hg38UCSC Ensembl
chr8:142159117..142167966hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg388850
hg198850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424688
Supporting Variants
Samples
Known GenesDENND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235112
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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