A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751669



Internal ID21386640
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 StatusS
Merged Variantsnsv4435748
Supporting Variants
SamplesMDQ025
Known GenesFBXO10, POLR1E
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751669
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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