A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485106



Internal ID262502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37814189..37818127hg38UCSC Ensembl
chr9:37814186..37818124hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg383939
hg193939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024787
Samples
Known GenesDCAF10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485106
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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