A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913302



Internal ID22688518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116760879..116774630hg38UCSC Ensembl
chr9:119523158..119536909hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3813752
hg1913752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447701
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913302
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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