A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509806



Internal ID20883118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75904493..76030101hg38UCSC Ensembl
chr15:76196834..76322442hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38125609
hg19125609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196484
Samples
Known GenesFBXO22, FBXO22-AS1, NRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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