A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435748



Internal ID21397750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37502004..37515003hg38UCSC Ensembl
chr9:37502001..37515000hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3813000
hg1913000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751669, nssv15752156
SamplesMDQ010, MDQ025
Known GenesFBXO10, POLR1E
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435748
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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